supervisor quality control

PCI Pharma Services

<div><div>Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.</div><div><br>
We are PCI.</div><div><br>
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.</div><div></div><div><br>
Summary of Objective:</div><div></div><div>
The QC Analytical Supervisor will have responsibility for supporting all activities in the Quality Control Laboratory including completing the majority of the peer review in the department and approving the majority of procedures used in the analytical department. The work includes the testing of in-process samples, finished product samples and raw materials. The QC Analytical Supervisor will communicate with clients regarding Out of Specification and other Quality System Events. The person in this position has knowledge of commonly-used analytic concepts, practices, and procedures within the field of his/her responsibilities. Also, must be familiar with cGMPs as they relate to analytical test methodologies and practices.</div><div>
Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following but other duties may be assigned.</div><ul><li><div>
Prioritize and distribute work to the analysts working in the QC Analytical laboratory</div></li><li><div>
Conduct OOS and customer complaint investigations</div></li><li><div>
Complete peer review of work executed within the analytical laboratory</div></li><li><div>
Train new Employees</div></li><li><div>
Routine Analytical testing of samples supporting incoming raw materials, in-process production and finished product testing</div></li><li><div>
Performs analytical testing using HPLC, Karl Fischer, Particle Size Analyzer, UV Vis, Densitometer, Osmometer and other instrumentation as required</div></li><li><div>
Perform instrument calibrations and preventative maintenance as needed Documents laboratory work using laboratory worksheets/notebooks. Documentation must be detailed and meet CGMP requirements</div></li><li><div>
Write, review and revise SOPs as required</div></li><li><div>
Other duties as assigned or required</div></li></ul><div></div><div>
Special Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must be physically capable to perform the duties listed below with or without reasonable accommodations which may be made to enable individuals with disabilities to perform the essential functions.</div><ul><li><div>
Routine work requires walking, standing, bending, reaching, climbing stairs, lifting or carrying objects that typically weigh less than 50 lbs.</div></li><li><div>
Capacity to work on several tasks simultaneously.</div></li><li><div>
Able to organize and prioritize work activities.</div></li><li><div>
Must be able to walk and drive between locations</div></li><li><div>
Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves</div></li><li><div>
Comfortable with working/handling of hazardous materials</div></li></ul><div></div><div><br>
Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</div><ul><li><div>
Works closely with Quality Assurance and Quality Control staff in performing varied work procedures and activities.</div></li><div></div><li><div>
Interacts with Operations staff, Research and Development staff and clients on a regular basis.</div></li><li><div>
Supervises the employees in the QC Analytical departmen</div></li><li><div>
TRAVEL &ndash; &lt;10%</div></li></ul><div></div><div><br>
Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</div><ul><li><div>
5+ years relevant Analytical Chemistry experience, preferably in Quality Control, in a pharmaceutical manufacturing company</div></li><li><div>
Experience working in a cGMP laboratory required</div></li><li><div>
Experience working in a CMO (contact manufacturing/development organization) preferred</div></li><li><div>
Prior leadership experience is preferred</div></li><li><div>
Bachelor of Science in a scientific area of study</div></li><li><div>
Master of Science in a scientific area of study and 3+ years Analytical Chemistry experience, preferably in Quality Control, in a pharmaceutical manufacturing company</div></li><li><div>
Ability to prioritize tasks for staff</div></li><li><div>
Ability to make informed decisions</div></li><li><div>
Detail oriented</div></li><li><div>
Strong oral and written communication skills</div></li><li><div>
Excellent organization skills</div></li><li><div>
Office Suite experience (Excel, Word, Access, and PowerPoint)Bachelor of Science in a scientific area of study</div></li></ul><ul><li><div>
Excellent interpersonal skills and the ability to communicate well both orally and in in writing</div></li><li><div>
Ability to multi-task in a dynamic environment with changing priorities</div></li><li><div>
Resilient, can quickly move forward despite challenges</div></li><li><div>
A drive to achieve results for self, and the team, and is cable of working with limited supervision</div></li><li><div>
Positive attitude and strong team, cross team collaboration</div></li><li><div>
Honesty, integrity, respect and courtesy with leadership and peers</div></li><li><div>
Strong commitment to conducting PCI PHARMA SERVICES business according to the highest legal and ethical standards, and to continually pursue excellence in the manufacturing and delivery of PCI PHARMA SERVICES products and services</div></li><li><div>
undefined</div></li></ul><div></div><div>
#LI-LL1</div><div></div><div>
Join us and be part of building the bridge between life changing therapies and patients. <div>Let&rsquo;s talk future</div></div><div></div><div>
Equal Employment Opportunity (EEO) Statement:<br>
<i>PCI Pharma Services is an Equal </i><i>Opportunity/Affirmative</i><i> Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.</i></div><div></div><div><i>
At PCI, Equity and Inclusion are at the core of our company&rsquo;s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity &ndash; at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.</i></div></div><div></div>

Supervisor, QC Analytical Wed to Sat 6:30 AM to 5PM

D.P. Jewellers

<div>
 <p>
  <strong>
   About the Company
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  D.P. Abhushan Ltd. is a trusted and renowned name in the Indian gems and jewellery industry, known for its exquisite craftsmanship, legacy of trust, and commitment to delivering timeless designs. With a strong presence in Central India, we are expanding our retail footprint and seeking passionate professionals to join our growing team.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   About the Role
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Job Title: Quality Control Head
 </p>
 <p>
  Job Type: Regular, Full-time
 </p>
 <p>
  Location: Mumbai, Maharashtra, India
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Job Summary:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  We are seeking a highly skilled and experienced Quality Control Head to join our team. The ideal candidate will be responsible for overseeing the quality control processes and procedures for our jewelry products. This role will be based at our Sourcing Office in Mumbai, Maharashtra, India.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities:
  </strong>
 </p>
 <p>
  - Develop and implement quality control processes and procedures for jewelry products.
 </p>
 <p>
  - Conduct regular quality audits to ensure compliance with company standards and industry regulations.
 </p>
 <p>
  - Collaborate with cross-functional teams to identify and resolve quality issues.
 </p>
 <p>
  - Train and mentor quality control team members to ensure consistent and accurate execution of quality control processes.
 </p>
 <p>
  - Monitor and analyze quality control data to identify trends and areas for improvement.
 </p>
 <p>
  - Develop and maintain relationships with suppliers to ensure quality standards are met.
 </p>
 <p>
  - Stay updated on industry trends and advancements in quality control practices.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications:
  </strong>
 </p>
 <p>
  - Bachelor's degree in a relevant field (e.g. engineering, quality management, etc.).
 </p>
 <p>
  - Minimum of 10 years of experience in quality control, preferably in the jewelry industry.
 </p>
 <p>
  - Strong knowledge of quality control processes and procedures.
 </p>
 <p>
  - Experience in conducting quality audits and analyzing data.
 </p>
 <p>
  - Excellent communication and interpersonal skills.
 </p>
 <p>
  - Ability to work in a fast-paced and dynamic environment.
 </p>
 <p>
  - Strong leadership and team management skills.
 </p>
 <p>
  - Attention to detail and a commitment to delivering high-quality products.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Equal Opportunity Statement
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  At D.P. Abhushan Ltd., we are committed to fostering a diverse and inclusive workplace. We believe that every individual deserves equal respect, opportunities, and fair treatment&mdash;regardless of gender, age, caste, religion, ethnicity, disability, marital status, or background.
 </p>
 <p>
  <br/>
 </p>
 <p>
  We are proud to be an
  <strong>
   Equal Opportunity Employer
  </strong>
  , and we strive to create an environment where talent thrives purely on the basis of merit, dedication, and performance.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Join us in building a workplace that reflects the values of respect, integrity, and equality.
 </p>
</div>


Head of Quality Control

INTERNATIONAL PHARMA LABS

<p>&middot; Sufficient samples of starting materials and products are retained to permit future examination of the product.</p><p>&middot; Complaints related to the quality of the product are investigated.</p><p>&middot; All tests and analysis conducted shall be in accordance with the instructions given in the relevant written test procedures. The result shall be checked by the supervisor before the material or product is released or rejected.</p><p>&middot; Identity from each container.-- An identity test shall be conducted on a sample from each container of starting material.</p><p>Records of testing.- In process control records shall be maintained and form a part of the batch records.To support QCM in all QC activities</p><p>To test raw materials, intermediates and finished products using current pharmacopoeias, any associated &lsquo;wet&rsquo; chemistry and instrumental techniques (HPLC, IR, UV), as appropriate.</p><p>To prepare Quality reports, including analytical reports (for raw materials and finished products), Certificates of Analysis (CoA) (for finished products) and stability reports and get them signed from QCM</p><p>To create and execute method development and method validation test protocols for finished products and generate the appropriate analytical methods</p><p>To conduct stability testing of products for new formulations and ongoing stability trials, using physical (pH, viscosity) and instrumental (HPLC, UV) techniques, as appropriate</p><p>To write analytical specifications using current pharmacopoeias and review existing analytical specifications</p><p>To write/review Standard Operating Procedures (SOPs) for QC Department</p><p>To calibrate analytical equipment, as and when required</p><p>To comply with company Standard Operating Procedures (SOPs)</p><p>To maintain laboratory equipment</p><p>To train the new laboratory personnel</p><p>To perform any other duty assigned by the line manager</p><p>To check and ensure the performance of gowning qualification for cleanroom personnel</p><p>To check and ensure the performance aseptic technique verification for new hires</p><p>To check and ensure the qualification of pharmacy tech (media fill), documentation, protocol and preparation of final reports</p><p>To check and ensure the performance and document growth promotion test</p><p>To check and ensure the maintenance microbiology laboratory equipment</p><p>To check and ensure the training of the new laboratory personnel</p><p>To check and ensure the maintenance the laboratory temperature logs including chemical and micro labs</p><p><b>To perform the following tasks as per the schedule BII checklist and have the data ready for presentation for the audit at all times</b></p><p>&middot; All necessary controls on starting materials, intermediate products, and bulk products and other in process controls calibrations are carried out;</p><p>&middot; Records are made that all the required inspecting and testing procedures have actually been carried out and that any deviation has been fully recorded and investigated;</p><p>Records are made of the results of inspecting and testing materials and intermediate, bulk against specifications and product assessment</p><p>Job Type: Full-time</p><p>Pay: Rs70,000.00 - Rs100,000.00 per month</p><p>Work Location: In person</p>

Deputy Quality Control

Join Parachute

<div><h3 class="jobSectionHeader"><b>Description</b></h3><div><br>
<b>
Who We Are:</b><br>
<br>
We&rsquo;re building a better way to donate plasma &mdash; one that&rsquo;s fast, friendly, and powered by smart technology - our donor app makes booking and earning easy for donors, and our team makes every visit feel welcoming and personal. We&rsquo;ve grown from 2 to 30+ locations in under 3 years, and we&rsquo;re just getting started. If you want to grow your career with a high-energy team, this is a great opportunity.<br>
<br>
<b>What You'll do:</b><br>
<br>
As the Center Quality Assurance Supervisor, you&rsquo;ll own the regulatory and compliance program at the Donor Center, ensuring it operates at the highest standards of compliance, accuracy, and safety. You will be a key part of our culture of quality, holding the team accountable while creating a positive environment for the team and our donors. You will have a unique opportunity to be part of a high-growth organization, one that is changing rapidly and creating new opportunities for our high-performing team members.<br>
</div><div><b>Compensation: </b>Up to $70K ($50K - $55K base + up to 25% monthly bonus) + benefits</div><div>
<b>Travel:</b> 8 weeks of paid training with travel and accommodations provided</div><h3 class="jobSectionHeader"><b><br>
Key Responsibilities</b></h3><br>
<ul>
<li>
Lead quality programs, including overseeing inspections, audits, and corrective action plans.</li>
<li>Keep the center audit-ready by maintaining compliance with industry, government, and company regulations at all times.</li>
<li>Provide independent oversight &ndash; maintain quality checks and documentation separate from daily operations to ensure objectivity.</li>
<li>Support center leadership &ndash; work closely with the Center Director to maintain safety and operational excellence.</li>
<li>Improve processes &ndash; track trends, analyze data, and implement plans to increase efficiency and reduce risk.</li>
<li>Oversee training and knowledge &ndash; ensure staff are trained and compliant with new policies and procedures.</li></ul><br>
<h3 class="jobSectionHeader"><b>
Required Qualifications</b></h3><br>
<ul>
<li>
3+ years of experience in a regulated or process-driven environment (e.g., manufacturing, clinical, or business settings)</li>
<li>High school diploma, GED equivalent, or higher education</li>
<li>Ability to lift 50 lbs., sit or stand for extended periods, and enter cold environments (-40&deg;C) for short periods</li>
<li>Ability to work day and evening hours, weekends, holidays and extended shifts as needed.</li>
</ul><div><b> Who You Are</b></div><ul>
<li>A Detail -Oriented Problem Solver &ndash; You take ownership. You're excited to get in the weeds, know how to creatively prioritize and solve a long, ambiguous, and evolving task list, are trustworthy and outcomes oriented</li>
<li>An Empathetic Communicator &ndash; You know how to adapt your communication style to meet different audiences (staff with different styles, donors, Ops leadership); you have strong conflict resolution skills, are even-keeled under pressure, and know how to motivate and inspire others</li>
<li>A Development-Minded Employee - You are self-aware and curious, have integrity, and have a track record of steep learning curves</li>
<li>A Data-Driven Decision Maker &ndash; You are metrics driven, have strong logical reasoning and decision-making skills, aren&rsquo;t distracted by one-offs or edge cases</li>
</ul><div>
<br>
 <b>Who You Are Not</b></div><ul>
<li><i>Someone who isn&rsquo;t excited to get their hands dirty </i>&ndash; while you are hired for a role, our operations are often unpredictable, and we need people willing to jump in where they&rsquo;re needed.</li>
<li><i>Someone who doesn&rsquo;t thrive in an environment of continuous change &ndash; </i>we are in a hypergrowth stage, which is unique for this industry. We need people who are excited to be with us on this rollercoaster.</li>
<li><i>Someone who wants to clock in and clock out.</i> We are looking for team players who care about the impact their centers have on their communities and the plasma-based medicine, which takes a true ownership mentality and often extra hours.</li></ul><br>
<h3 class="jobSectionHeader"><b>
Why Join Parachute?</b></h3><br>
<ul>
<li>
Competitive compensation with bonus potential</li>
<li>Medical, Dental, and Vision insurance</li>
<li>Paid time off</li>
<li>Company paid holidays</li>
<li>Career growth opportunities</li></ul><div></div><h3 class="jobSectionHeader"><b><br>
About Join Parachute</b></h3><div>
Parachute is a new kind of plasma donation company that allows individuals to earn money while creating life-saving medicine.<br>
</div><div>Plasma is used to create medicine that treats chronic illnesses, including immune disorders, liver disease, bleeding disorders, and cancer. Right now, there&rsquo;s a severe plasma shortage, which is impacting patients&rsquo; access to these life-saving treatments.</div></div>

Center Quality Assurance Supervisor

<div><h3 class="jobSectionHeader"><b>Description</b></h3><div><br>
<b>
Who We Are:</b><br>
<br>
We&rsquo;re building a better way to donate plasma &mdash; one that&rsquo;s fast, friendly, and powered by smart technology - our donor app makes booking and earning easy for donors, and our team makes every visit feel welcoming and personal. We&rsquo;ve grown from 2 to 30+ locations in under 3 years, and we&rsquo;re just getting started. If you want to grow your career with a high-energy team, this is a great opportunity.<br>
<br>
<b>What You'll do:</b><br>
<br>
As the Center Quality Assurance Supervisor, you&rsquo;ll own the regulatory and compliance program at the Donor Center, ensuring it operates at the highest standards of compliance, accuracy, and safety. You will be a key part of our culture of quality, holding the team accountable while creating a positive environment for the team and our donors. You will have a unique opportunity to be part of a high-growth organization, one that is changing rapidly and creating new opportunities for our high-performing team members.
<br>
<br>
<b>Compensation: </b>Up to $70K ($50K - $55K base + up to 25% monthly bonus) + benefits</div><div>
<b>Travel:</b> 8 weeks of paid training with travel and accommodations provided</div><h3 class="jobSectionHeader"><b><br>
Key Responsibilities</b></h3><br>
<ul>
<li>
Lead quality programs, including overseeing inspections, audits, and corrective action plans.</li>
<li>Keep the center audit-ready by maintaining compliance with industry, government, and company regulations at all times.</li>
<li>Provide independent oversight &ndash; maintain quality checks and documentation separate from daily operations to ensure objectivity.</li>
<li>Support center leadership &ndash; work closely with the Center Director to maintain safety and operational excellence.</li>
<li>Improve processes &ndash; track trends, analyze data, and implement plans to increase efficiency and reduce risk.</li>
<li>Oversee training and knowledge &ndash; ensure staff are trained and compliant with new policies and procedures.</li></ul><br>
<h3 class="jobSectionHeader"><b>
Required Qualifications</b></h3><br>
<ul>
<li>
3+ years of experience in a regulated or process-driven environment (e.g., manufacturing, clinical, or business settings)</li>
<li>High school diploma, GED equivalent, or higher education</li>
<li>Ability to lift 50 lbs., sit or stand for extended periods, and enter cold environments (-40&deg;C) for short periods</li>
<li>Ability to work day and evening hours, weekends, holidays and extended shifts as needed.</li>
</ul><div><b> Who You Are</b></div><ul>
<li>A Detail -Oriented Problem Solver &ndash; You take ownership. You're excited to get in the weeds, know how to creatively prioritize and solve a long, ambiguous, and evolving task list, are trustworthy and outcomes oriented</li>
<li>An Empathetic Communicator &ndash; You know how to adapt your communication style to meet different audiences (staff with different styles, donors, Ops leadership); you have strong conflict resolution skills, are even-keeled under pressure, and know how to motivate and inspire others</li>
<li>A Development-Minded Employee - You are self-aware and curious, have integrity, and have a track record of steep learning curves</li>
<li>A Data-Driven Decision Maker &ndash; You are metrics driven, have strong logical reasoning and decision-making skills, aren&rsquo;t distracted by one-offs or edge cases</li>
</ul><div>
<br>
 <b>Who You Are Not</b></div><ul>
<li><i>Someone who isn&rsquo;t excited to get their hands dirty </i>&ndash; while you are hired for a role, our operations are often unpredictable, and we need people willing to jump in where they&rsquo;re needed.</li>
<li><i>Someone who doesn&rsquo;t thrive in an environment of continuous change &ndash; </i>we are in a hypergrowth stage, which is unique for this industry. We need people who are excited to be with us on this rollercoaster.</li>
<li><i>Someone who wants to clock in and clock out.</i> We are looking for team players who care about the impact their centers have on their communities and the plasma-based medicine, which takes a true ownership mentality and often extra hours.</li></ul><br>
<h3 class="jobSectionHeader"><b>
Why Join Parachute?</b></h3><br>
<ul>
<li>
Competitive compensation with bonus potential</li>
<li>Medical, Dental, and Vision insurance</li>
<li>Paid time off</li>
<li>Company paid holidays</li>
<li>Career growth opportunities</li></ul><div></div><h3 class="jobSectionHeader"><b><br>
About Join Parachute</b></h3><div>
Parachute is a new kind of plasma donation company that allows individuals to earn money while creating life-saving medicine.<br>
</div><div>Plasma is used to create medicine that treats chronic illnesses, including immune disorders, liver disease, bleeding disorders, and cancer. Right now, there&rsquo;s a severe plasma shortage, which is impacting patients&rsquo; access to these life-saving treatments.</div></div>

Search 10000+ Supervisor quality control jobs near you this November. New roles added regularly across leading industries. Apply today.

10000 supervisor quality control jobs NEAR_ME

Supervisor, QC Analytical Wed to Sat 6:30 AM to 5PM

Head of Quality Control

Deputy Quality Control

Center Quality Assurance Supervisor

Center Quality Assurance Supervisor

Center Quality Assurance Supervisor

Center Quality Assurance Supervisor