associate scientist

Syngene International Limited

<div>
 Date: 5 Feb 2026
 <br/>
 <br/>
 Location:
 <br/>
 <br/>
 Bangalore, KA, IN, 560099
 <br/>
 <br/>
 Division: Dedicated Centre
 <br/>
 <br/>
 <strong>
  JOB DESCRIPTION
 </strong>
 <strong>
  Designation:
 </strong>
 Associate Scientist
 <strong>
  Job Location:
 </strong>
 Bangalore
 <strong>
  Department:
 </strong>
 DDS SATT
 <strong>
  About Syngene
 </strong>
 Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene&rsquo; s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&amp;D productivity, speed up time to market and lower the cost of innovation.
 <br/>
 <br/>
 <strong>
  Key Responsibilities:
 </strong>
 The successful candidate will become a member of a team with overall responsibility for purification and analysis of small compound libraries to support lead optimization in medicinal chemistry programs. Individual responsibilities will include analysis and purification of small molecule library compounds (primarily by analytical and preparative LCMS), HPLC and mass spectrometer instrument maintenance, training, and analytical data management. Optimization and/or troubleshooting of analysis conditions will be required to ensure on time delivery of high purity products.
 <br/>
 <br/>
 <strong>
  Educational Qualification:
 </strong>
 M.Sc. in Chemistry/Analytical chemistry with experience in practical analytical chemistry, including both analysis and purification.
 <strong>
  Required Skills:
 </strong>
 Knowledge and expertise in preparative HPLC, LCMS, and other chromatographic techniques is desirable. Strong computer skills and good communication skills, are preferable. Demonstrated ability to work in a highly team oriented, multitasking environment with experience in technology enabled analysis and purification will be highly appreciated.
 <strong>
  Behavioral Skills:
 </strong>
 Good communication skills, good presentation skills, hardworking, sincere and a team player. Must demonstrate integrity and take accountability of their work
 <strong>
  Equal Opportunity Employer:
 </strong>
 It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.
</div>


ASSOCIATE SCIENTIST

Pfizer

<div><div>Why Patients Need You</div><div></div><div>
Pfizer&rsquo;s purpose is to deliver breakthroughs that change patients&rsquo; lives. Research and Development is at the heart of fulfilling Pfizer&rsquo;s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy, or supporting clinical trials; you will apply cutting edge design and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world.</div><div></div><div>
What You Will Achieve</div><div></div><div>
As an Associate Scientist, you will be at the center of our operations and you&rsquo;ll find that everything we do, every day, is in line with an unwavering commitment to quality. Your work in the Analytical R&amp;D Microbiology Strategy &amp; Testing organization helps enable development of biological therapeutics at Pfizer. Your responsibilities will be applying GMP microbiological methods (bioburden, endotoxin, PCR, etc.) in the assessment of product quality and detection of impurities. Your contributions are part of a group performing microbiology identification, testing, and method qualifications to support multiple sites in the Pfizer network. You will be responsible for Environmental Monitoring (EM) of manufacturing facilities, waters, and compressed gases at the site. The Associate Scientist is responsible for utilizing established microbiological methodologies to support GMP in-process and research &amp; development testing of clinical supplies. You will become proficient in aseptic lab technique and facility gowning to thrive in this fast-paced environment. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. It is your focus and commitment that will help in making Pfizer ready to achieve new milestones and help patients across the globe.</div><div></div><div><br>
How You Will Achieve It</div><ul><li><div>
Exercise and build basic team effectiveness skills {e.g., commitment, feedback, consensus management) within the work group.</div></li><li><div>
Review and contribute to technical documents, including validation protocols and reports, analytical test procedures, investigation reports, monitoring trend reports, and change controls.</div></li><li><div>
Directly interact with multiple department team members, including presentation of data.</div></li><li><div>
Complete all Good Manufacturing Practice {part of G<i>x</i>P} and safety training in compliance with departmental requirements and follow appropriate safety practices in the workplace.</div></li><li><div>
Perform various experiments for microbial analysis, qualification/validation, and characterization of biological therapeutics.</div></li><li><div>
Perform and document environmental monitoring of manufacturing areas and related Microbiological activities.</div></li><li><div>
Conduct all work according to appropriate Standard Operating Procedures following Good Manufacturing Practices/Good Laboratory Practices (GMP/GLP) requirements and ensure integrity of all data generated and documented.</div></li><li><div>
Independently analyze and provide conclusions regarding data generated.</div></li><li><div>
Plan and prioritize assigned testing activities.</div></li><li><div>
Present problems and propose solutions in discussions with group members.</div></li></ul><div></div><div><br>
Qualifications</div><div>
Must-Have</div><ul><li><div>
Bachelor's degree in microbiology, biochemistry, biology, or related field with 0 to 2 years of experience</div></li><li><div>
Excellent documentation skills with high attention to detail</div></li><li><div>
Strong organizational skills and effective interpersonal and written communication skills</div></li><li><div>
Self-motivated and highly effective in a team-based environment</div></li><li><div>
Ability to follow established procedures under minimal supervision</div></li></ul><div></div><div>
Nice-to-Have</div><ul><li><div>
1+ years&rsquo; experience with Quality Systems in a Good Manufacturing Practices (GMP) environment</div></li><li><div>
Experience with laboratory data systems such as Laboratory Information Management Systems (LIMS)</div></li><li><div>
Hands on experience or working knowledge in pharmaceutical industry and handling of analytical instruments</div></li><li><div>
Some knowledge of drug development process for progression of biological candidates</div></li></ul><div></div><div>
PHYSICAL/MENTAL REQUIREMENTS</div><div></div><div>
Position requires occasional light lifting and periods of standing, sitting or walking. Laboratory testing involves repetitive operations using hand-held instruments (micropipettes).</div><div></div><div>
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS</div><div></div><ul><li><div>
This is typically a Monday-Friday schedule, first shift. Occasional weekend work or off-shift hours work is required per business need.</div></li><li><div>
Candidate must be able to qualify on cleanroom gowning to conduct weekly monitoring of the manufacturing areas.</div></li></ul><div><br>
Work Location Assignment: On Premise</div><br>
<div></div>
The annual base salary for this position ranges from $60,200.00 to $97,500.00. In addition, this position is eligible for participation in Pfizer&rsquo;s Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life&rsquo;s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site &ndash; U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.<div></div><div>
Relocation assistance may be available based on business needs and/or eligibility.</div><div></div><div><div><div><div><div><div><div><div><div>
Sunshine Act</div><div>
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider&rsquo;s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</div></div></div></div></div></div></div></div></div><div></div><div><div><div><div><div><div><div><div><div>
EEO &amp; Employment Eligibility</div><div>
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.</div><div></div><div>
Pfizer endeavors to make <div>www.pfizer.com/careers</div> accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email <div>disabilityrecruitment@pfizer.com</div>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</div></div></div></div></div></div></div></div></div><div></div>
Research and Development</div><div></div>

Associate Scientist, Microbiology

CPS, Inc.

<div>
 Under direct supervision, this role leads the formula design, validation and implementation of new products, line extensions, product improvements and cost savings initiatives. This role will also serve as technical assistance to the manufacturing sites and supervisor.
 <br/>
 <br/>
 <strong>
  Essentials For This Role:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Under direct supervision, define the formulation, nutritional and process parameters needed to develop a new product which meets customer expectations and project objective(s)
  </li>
  <li>
   Work collaboratively in the execution of development from bench to production scale for new products, product improvements and cost savings projects
  </li>
  <li>
   Create new prototypes for product development initiatives and identify, evaluate and approve potential ingredients and manufacturing suppliers
  </li>
  <li>
   Identify opportunities for competitive market advantage through product benchmarking
  </li>
  <li>
   Contribute significantly, directly and continually to attain results through the generation and application of advanced, specialized knowledge
  </li>
  <li>
   Understand product requirements, plant equipment and processes to enable the creation of detailed product specifications
  </li>
  <li>
   Understand the commercialization process and contribute to the organization, implementation and management of work streams
  </li>
  <li>
   Generate and support pipeline work to drive cost optimization through formulation and processing efficiencies
  </li>
  <li>
   Manage calibration of laboratory equipment
  </li>
  <li>
   Work collaboratively with managers and teammates at other locations to execute individual and team goals
  </li>
  <li>
   Exhibit strong communication skills within technical and non-technical community
  </li>
  <li>
   If you&rsquo;d like to hear more about this opportunity and others we are currently working on, please contact Kristine O&rsquo;Sullivan at kosullivan@cps4jobs.com.
   <br/>
   <br/>
  </li>
 </ul>
 JO: 4.26KO
 <br/>
 <br/>
 Salary
 <br/>
 <br/>
 $65,000 - $75,000
 <br/>
 <br/>
 Benefits Available
 <br/>
 <br/>
</div>


Associate Scientist

Pace® Labs

<div>
 <strong>
  Shift
  <br/>
  <br/>
 </strong>
 Monday through Friday, 8:00 AM - 5:00 PM
 <br/>
 <br/>
 Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives.
 <br/>
 <br/>
 <strong>
  Summary
  <br/>
  <br/>
 </strong>
 Responsible for providing or overseeing the analysis, administration and oversight of standard chemistry/biochemistry policies, programs and practices; feedback and guidance regarding the analysis of samples using fundamental professional and technical knowledge of chemistry/biochemistry or related instrumentation, wet chemistry testing, and procedures.
 <br/>
 <br/>
 <strong>
  NOTE: This is an Evergreen role where we are collecting resumes for future openings
  <br/>
  <br/>
 </strong>
 Compensation: $28.00 per hour
 <br/>
 <br/>
 <strong>
  Essential Functions
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Provides fundamental analysis in support of standard testing materials, products and/or devices utilizing standard analytical instrumentation; follows Standard Operating Procedures and methods to perform testing.
  </li>
  <li>
   Provides fundamental review, analysis, interpretation, and documentation of testing results.
  </li>
  <li>
   Overseeing or reviewing, completing, and processing various types of standard chemistry/biochemistry forms, documents, databases, and related materials and information.
  </li>
  <li>
   Provides fundamental analysis and interpretation and counsel to staff, management, and functional leaders regarding chemistry/biochemistry policies, programs, and practices; involves standard operations.
  </li>
  <li>
   Provides standard research, feedback, and decisions to resolve management and employee questions and requirements; assists with receiving customer feedback and coordinating resources and responses as required.
  </li>
  <li>
   Analyzes and reviews process, results, feedback, and related chemistry/biochemistry information on an ongoing to as needed basis to determine trends, draw conclusions, interpret findings, and presents results, proposals, and recommendations to management.
  </li>
  <li>
   Ensures the accuracy of more fundamental tests, equipment, actions, procedures and operational databases, reports, and related details through audits, queries, and operational reviews; works with teams to resolve discrepancies; resolves discrepancies or escalates discrepancies to ensure quality assurance in testing process/results.
  </li>
  <li>
   Assists with developing or participating in chemistry/biochemistry or cross functional project or program objectives, which includes proposed budgets, timelines, materials, personnel, and other project requirements, receives direction, and presents information to management.
  </li>
  <li>
   Cleans, maintains, prepares, and calibrates equipment, samples, and related areas.
  </li>
  <li>
   Interprets and applies department policies and procedures and assists with applicable laws, rules, and regulations; receives guidance within these areas as needed.
  </li>
  <li>
   Contributes to the efficiency and effectiveness of the department's service to its customers by offering suggestions and directing or participating as an active member of a work team.
  </li>
  <li>
   Promotes and supports the overall mission of Pace Analytical by demonstrating courteous and cooperative behavior when interacting with customers and staff; acts in a manner that promotes a harmonious and effective workplace environment.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <strong>
  Education and Experience
  <br/>
  <br/>
 </strong>
 Bachelor's degree in chemistry/biochemistry, or a closely related field; OR an equivalent combination of education, training, and experience.
 <br/>
 <br/>
 <strong>
  Required Knowledge
  <br/>
  <br/>
 </strong>
 <strong>
  Required Knowledge and Skills
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Fundamental principles, practices, and techniques of chemistry/biochemistry.
  </li>
  <li>
   Standard understanding of the administration and oversight of chemistry/biochemistry programs, policies, and procedures.
  </li>
  <li>
   Fundamental methods to resolve chemistry/biochemistry problems, questions, and concerns.
  </li>
  <li>
   Standard understanding of applicable chemistry/biochemistry laws, codes, and regulations.
  </li>
  <li>
   Understanding of standard testing tools, instruments, and calibration.
  </li>
  <li>
   Computer applications and systems related to the work.
  </li>
  <li>
   Principles and practices to serving as an effective project team member.
  </li>
  <li>
   Methods to communicate with staff, coworkers, and customers to ensure safe, effective, and appropriate operations.
  </li>
  <li>
   Correct business English, including spelling, grammar, and punctuation.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Required Skills
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Performing fundamental professional-level chemistry/biochemistry duties in a variety of assigned areas.
  </li>
  <li>
   Overseeing and administering standard chemistry/biochemistry functions.
  </li>
  <li>
   Training others in policies and procedures related to the work.
  </li>
  <li>
   Serving as a team member and the development and management of projects.
  </li>
  <li>
   Operating in a both a team and individual contributor environment.
  </li>
  <li>
   Interpreting, applying, and explaining applicable laws, codes, and regulations.
  </li>
  <li>
   Preparing fundamental functionals reports, correspondence, and other written materials.
  </li>
  <li>
   Using initiative and independent judgment within established department guidelines.
  </li>
  <li>
   Using tact, discretion, and prudence in working with those contacted in the course of the work.
  </li>
  <li>
   Performing effective oral presentations to large and small groups across functional peers and the department.
  </li>
  <li>
   Contributing effectively to the accomplishment of team or work unit goals, objectives and activities.
  </li>
  <li>
   Establishing and maintaining effective working relationships with a variety of individuals contacted in the course of the work.
   <br/>
   <br/>
  </li>
 </ul>
 Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work.
 <br/>
 <br/>
 <strong>
  Benefits
  <br/>
  <br/>
 </strong>
 When you join Pace&reg;, you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft.
 <br/>
 <br/>
 <em>
  <strong>
   Equal Opportunity Employer
   <br/>
   <br/>
  </strong>
 </em>
 <em>
  Pace&reg; provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
 </em>
</div>


Associate Scientist I

Actalent

<div>
 <strong>
  Associate Scientist/Chemist
  <br/>
  <br/>
 </strong>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 We are seeking dedicated Chemists to perform routine tests on various samples, including finished products, stability samples, raw materials, and more using techniques such as UV and HPLC in a regulated laboratory environment. The role involves evaluating test results, maintaining accurate lab documentation, and ensuring compliance with SOPs and cGMP standards.
 <br/>
 <br/>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution.
  </li>
  <li>
   Evaluate test results and determine the acceptability of samples based on the results.
  </li>
  <li>
   Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs.
  </li>
  <li>
   Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards.
  </li>
  <li>
   Review notebooks promptly and ensure compliance with SOPs.
  </li>
  <li>
   Analyze and interpret results in both written and oral formats.
  </li>
  <li>
   Assist in training new analysts.
  </li>
  <li>
   Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.
  </li>
  <li>
   Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Essential Skills
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Proficiency in HPLC, UPLC, and UV-Vis techniques.
  </li>
  <li>
   Strong analytical Experience in chemistry.
  </li>
  <li>
   Familiarity with FDA and GMP regulations.
  </li>
  <li>
   Ability to analyze and interpret complex data.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Additional Skills &amp; Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master&rsquo;s degree with 1 year of experience.
  </li>
  <li>
   Problem-solving skills involving several concrete variables in standardized situations.
  </li>
  <li>
   Ability to perform necessary computations and interpret graphs.
  </li>
  <li>
   Working knowledge of instrumentation software used in laboratories.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Work Environment
  <br/>
  <br/>
 </strong>
 This position is based in a lab environment regulated by FDA and GMP standards.
 <br/>
 <br/>
 <strong>
  Job Type &amp; Location
  <br/>
  <br/>
 </strong>
 This is a Contract to Hire position based out of Fort Lauderdale, FL.
 <br/>
 <br/>
 <strong>
  Pay And Benefits
  <br/>
  <br/>
 </strong>
 The pay range for this position is $29.00 - $35.00/hr.
 <br/>
 <br/>
 Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 <br/>
 <br/>
 <ul>
  <li>
   Medical, dental &amp; vision
  </li>
  <li>
   Critical Illness, Accident, and Hospital
  </li>
  <li>
   401(k) Retirement Plan &ndash; Pre-tax and Roth post-tax contributions available
  </li>
  <li>
   Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
  </li>
  <li>
   Short and long-term disability
  </li>
  <li>
   Health Spending Account (HSA)
  </li>
  <li>
   Transportation benefits
  </li>
  <li>
   Employee Assistance Program
  </li>
  <li>
   Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Fort Lauderdale,FL. Application Deadline This position is anticipated to close on Feb 23, 2026.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  About Actalent
  <br/>
  <br/>
 </strong>
 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 <br/>
 <br/>
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 <br/>
 <br/>
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
</div>


Scientist/chemist/ QC/Associate Scientist

AbbVie

<div>
 <strong>
  Company Description
  <br/>
  <br/>
 </strong>
 AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas &ndash; immunology, oncology, neuroscience, and eye care &ndash; and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
 <br/>
 <br/>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <strong>
  Purpose:
  <br/>
  <br/>
 </strong>
 The Associate QC Scientist performs laboratory testing within a fast paced GMP environment in support of one or more of the following areas; raw materials, in-process product, final Bulk product, stability, and/or validation. Analyzes test data and evaluates results. Writes procedures with guidance. Works under the guidance of a supervisor but is able to manage time efficiently in achieving timely completion of assigned duties. Assists in trending data to support assay performance. Assists in writing lab Investigation reports.
 <br/>
 <br/>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Perform routine tasks competently and independently, and generate reliable and consistent results.
  </li>
  <li>
   Analyze and critique results, noting significant deviations.
  </li>
  <li>
   Troubleshoot experiments and instrumentation.
  </li>
  <li>
   Learn and understand new experimental techniques.
  </li>
  <li>
   Demonstrate skill in multiple techniques and appropriately modify protocols, as required, to suit the changing needs of research or development sciences.
  </li>
  <li>
   Place data in proper scientific context by consulting and citing relevant literature.
  </li>
  <li>
   Demonstrate technical proficiency in his/her field.
  </li>
  <li>
   Impact projects predominantly through lab and/or pilot plant based activities.
  </li>
  <li>
   Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree.
  </li>
  <li>
   2+ years of related work experience
  </li>
  <li>
   Maintains their certifications as needed for assigned job tasks.
   <br/>
   <br/>
  </li>
 </ul>
 Additional Information
 <br/>
 <br/>
 Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
 <br/>
 <br/>
 <ul>
  <li>
   The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  </li>
  <li>
   We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  </li>
  <li>
   This job is eligible to participate in our short-term incentive programs.
   <br/>
   <br/>
  </li>
 </ul>
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Associate Scientist, Quality Control

A-TEK Inc

<div><div><p><b>Empower, Innovate, Impact!</b> At Team A-TEK, we EMPOWER people to drive INNOVATION that IMPACTS mission!</p>
<p>
A-TEK operates at the intersection of mission and innovation by applying our deep domain expertise across the federal markets. Embracing our digital-first strategy, A-TEK provides enhanced capabilities in application development, digital transformation, enterprise IT, and scientific services. Our solutions are designed to modernize, automate, secure, protect, and enhance the operations of our federal clients, ensuring they stay ahead in a rapidly evolving digital landscape.</p>
<p>
Our work is fueled by a passion to serve our clients' needs and to protect the safety and welfare of Americans. That passion shapes how we nurture our most valuable asset &ndash; Our Employees. A-TEK actively cultivates the talent that drives our success and fosters a creative, challenging, and mission-driven work environment for current and future employees.</p></div><p></p><p><br>
This position will be responsible for performing non-research molecular testing of samples for potentially containing biological threat agents. Ensures incoming operational, QA, and other sample types are processed while maintaining chain of custody. Prepares reports, answers questions, troubleshoots, and makes recommendations to the supervisor for inclusion in comprehensive reports. Maintains and operates equipment properly and in a safe manner, including performing routine calibrations and adjustments. Performs all procedures in accordance with proper handling and storage of various materials. Additionally, will be responsible for maintaining knowledge and skills related to position and program. Laboratory operations are 7 days a week. Team members take turns with weekends and holidays to ensure results are reported each day. In the event of a public health emergency, extended work hours and alternative shift work may be required to maintain temporary emergency 24/7 operations. Kindly be aware that a pre-employment drug screening is a requirement.</p>
<p><b>
REQUIRED QUALIFICATIONS:</b></p>
<p>
Bachelor's degree from an accredited university in microbiology, molecular biology, or related course work in biological sciences.</p>
<p><b>
REQUIRES</b> at least one year of laboratory bench experience, utilizing PCR, aseptic techniques and experience with biological assays. Laboratory training that is assigned or accompanies an associated course is not considered applicable training</p>
<p>
This position supports a federal contract which requires that all employees and job applicants hold a valid Green Card or US Citizenship at the time of application.</p><p></p><div>
<p>
Candidates may use tools (including AI) for proofreading or formatting; however, using any tool to fabricate, exaggerate, or misrepresent qualifications, experience, or work product is not permitted. We may assess application materials for job-related technical depth, internal consistency, and demonstrated hands-on experience, including through follow-up questions, skills assessments, or reference checks.</p>
<p>
Misrepresentation or falsification may result in removal from further consideration. Candidates who need a reasonable accommodation in the application or interview process may request one.</p>
<p><b>
A-TEK, Inc. is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or status as a qualified individual with a disability, or Vietnam era or other protected Veteran status. </b><b>Verification of education may be requested before or during the hiring process.</b></p></div></div>

Associate Scientist I Miami

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