Urwah Admin

Pfizer

<div><div>Use Your Power for Purpose</div><div></div><div>
You&rsquo;ve just received life changing news&hellip;cancer! The doctor recommends several rounds of chemotherapy. Unfortunately, chemotherapy not only targets the cancerous cells but the healthy tissues as well. During chemotherapy treatments, you experience fatigue, immunosuppression to other diseases, nausea/vomiting, hair loss, and other symptoms. What if there was a way to deliver that cytotoxic drug directly to the cancerous cells and not indiscriminately to healthy cells across the body, significantly reducing the adverse effects observed with chemotherapy? Pfizer is at the forefront of antibody-drug conjugates (ADCs) biotherapeutic development. ADCs attach a cytotoxic drug (monomethyl auristatin E or MMAE) directly to an antibody which is released upon uptake into the tumor-expressing cell killing it. This novel technology significantly minimizes the impact to healthy cells, thus reducing the toxic effects observed in chemotherapy and being a far more effective way to treat patients and increase survivability to life altering diagnosis.</div><div></div><div>
Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.</div><div></div><div>
What You Will Achieve</div><div></div><div>
In this role, you will:</div><div></div><div>
The position will support the Pfizer Sanford, NC Quality Operations department by performing Quality Control activities associated with clinical and/or commercial product, raw materials, and validation. Key responsibilities are performing GMP tasks associated with maintaining compliant Quality Control and Stability laboratories; testing, analyzing, interpreting, and trending results; and creating, reviewing and approving documentation.</div><div></div><div>
Individual should have knowledge of current Good Manufacturing Practices (cGMP), Laboratory Information Management System (LIMS), Microsoft Office&trade; applications specifically Word and Excel, analytical techniques and instrumentation, Lean Six Sigma concepts, and Lean Labs.</div><div></div><div><br>
At a minimum, the individual should be considered able to demonstrate the following:</div><ul><li>
Acts safely and follows all EH&amp;S safety requirements for site and QC laboratories.</li><li>
Be recognized as a &ldquo;go-to&rdquo; person or Subject Matter Expert for a specific subject area and are considered capable of supporting audits and investigations, reviewing/approving technical content to ensure scientific merit and compliance to regulations and Pfizer policy and standards.</li><li>
Excellent written and verbal communication skills</li><li>
Ability to identify issues, present complex problems with possible solutions, and actively take a leadership role to resolve issues.</li><li>
Ability to solve highly complex mathematical problems and situation-dependent problems using convoluted information.</li><li>
Ability to receive feedback from management and colleagues and take accountability for actions and personal development.</li><li>
Aptitude for good decision making based on procedures, guidance, and experience.</li><li>
Awareness to know their own limitations and seek senior scientist or management guidance when appropriate.</li><li>
Desire to ensure correctness and accuracy in tasks and documentation.</li><li>
Fitness of functioning as a team member and performing independent work with minor guidance</li><li>
Willingness to use personal skills and knowledge to achieve individual and company goals and objectives.</li><li>
Understanding of own area of function and knowledge of other cross functional areas</li><li>
Able to create, review, and approve test method and/or equipment validation records with limited guidance/coaching.</li><li>
Understands the importance of feedback and receives feedback well from management and other colleagues.</li><li>
Makes good decisions based on knowledge of quality systems and technical experience.</li><li>
Recognizes the impact of procedural changes that may impact future quality tasks and decisions.</li><li>
Able to review working instructions for technical content within own subject area and reference to applicable GMPs and regulatory expectations.</li><li>
Responsible for personal timelines and seeks advice if conflicts arise.</li><li>
Interacts with business lines and shares information with team; capable of influencing and negotiating with business lines.</li><li>
Ability to communicate effectively with good interpersonal skills.</li><li>
Perform tasks associated with maintaining Good Manufacturing Practices (cGMP) compliant Quality Control and Stability laboratories.</li><li>
Support routine testing and analysis of batch samples associated with vary modalities in a QC setting.</li><li>
Follow Environment Health and Safety requirements for site and QC laboratories.</li><li>
Perform complex mathematical problems and data analysis.</li><li>
Support product transfers, new product development, regulatory queries, cost improvement projects, and Drug Product plant support for Cleaning Validation.</li><li>
Operate within established HR policies and basic colleague relations guidelines.</li><li>
Write Standard Operating Procedures (SOPs), technical reports, project plans, etc.</li></ul><div></div><div><br>
Here Is What You Need (Minimum Requirements)</div><ul><li>
Applicant must have a bachelor's degree with 0+ years of experience; OR an associate's degree with 4 years of experience; OR a high school diploma (or equivalent) and 6 years of relevant experience.</li><li>
Demonstrated knowledge of manufacturing, quality or engineering practices in the biotech or pharmaceutical industry</li><li>
Aptitude for good decision making based on procedures, guidance, and experience.</li><li>
Effective communication skills</li><li>
Knowledge of Microsoft Office applications, specifically Word and Excel</li><li>
Excellent effective written and verbal communication and interpersonal skills</li><li>
Ability to work in a team environment.</li></ul><div></div><div>
Bonus Points If You Have (Preferred Requirements)</div><ul><li>
Relevant experience in biotherapeutics (antibodies, vaccines, and gene therapy)</li><li>
Experience with Laboratory Information Management System (LIMS)</li></ul><div></div><div><br>
Physical/Mental Requirements</div><ul><li><div>
Ability to lift 30 lbs, stand for 2 to 3 hours at a time, sit for 2 to 3 hours at a time, walk long distances and bend to obtain items from lower shelving/cabinets.</div></li></ul><ul><li><div>
Intellectual capability to perform complex mathematical problems and perform complex data analysis.</div></li></ul><div></div><div>
Non-Standard Work Schedule, Travel or Environment Requirements</div><div></div><ul><li><div>
Work schedule is first shift (8:00 am to 4:30 pm) but can include weekdays and/or weekend days as appropriate for assigned tasks/activities. Minimal flexibility in work schedule to cover business needs. Minimal off-shift work to ensure business needs are met.</div></li></ul><ul><li><div>
Non-existent to minimal travel.</div></li></ul><ul><li><div>
Must be able to wear appropriate PPE (e.g., lab coat, safety glasses, non-porous shoes, gloves, etc.)</div></li></ul><div><br>
Work Location Assignment: On Premise</div><div></div><div>
OTHER JOB DETAILS</div><div>
Last Date to Apply for Job: June 4th, 2025<br>
Referral Bonus Eligibility: YES<br>
Eligible for Relocation Package: NO</div><div></div>
The annual base salary for this position ranges from $66,500.00 to $110,900.00. 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></div></div></div></div></div><div></div>
Quality Assurance and Control<div></div>
#LI-PFE</div>

Job Id: I4sYIwk9NQbedCRAUp//UYpTpHjA9UvMOpt7i1WSA5oN4Kc1ewjyal086Odq7pBSlqL1jvc2wws+9tsYv8dBb1Iv/Yn7ozHU3E79TGnafaEykkV3W3hjakT8oo3lO75bPZLZyXm8cfvbXbIg6ZgZCeSNG7bGhqXH9qPlOMyM0Dkg1c3U7Q5K8PY1U/paBFG8+S0oZx2RuZv31eU8Nd1K2PhkjxE5g23N7eWuaAVu3fM=

Sr. Associate Scientist, QC Chemistry

<div><div>Role Summary</div><div></div><div>
The QC Lab Analyst II, will perform basic analysis for raw materials, in process and finished products a safe, compliant, and efficient manner. The Job responsibilities include performing wet chemistry and analytical testing to evaluate the quality of the incoming raw materials and analyze the finished product to demonstrate that the quality of our products meet the high standards of quality.</div><div>
Report testing results through computerized systems, or through standard laboratory paper-based documentation. Other related duties essential to these operations or special assignments as required.</div><div></div><div>
Role Responsibilities</div><ul><li><div>
Consistently adheres to company, site, and laboratory safety rules and immediately raises any safety issues with supervision as soon as they are identified.</div></li><li><div>
Follows procedures at all times, adopting cGMP, cGDP practices.</div></li><li><div>
Follows supervisor directions at all times.</div></li><li><div>
Able to function independently, but asks questions as necessary</div></li><li><div>
Accepts dynamic work sequences</div></li><li><div>
Must be self-motivated and work with minimal direction</div></li><li><div>
Demonstrate proficiency in computerized systems (Experience and use of LIMS, Empower are plus).</div></li><li><div>
Demonstrated ability to troubleshoot analytical methods</div></li><li><div>
Actively participates in daily and weekly planning discussions with his/her teammates and supervision (as needed) offering suggestions to improve RFT and schedule adherence as needed</div></li><li><div>
Works with supervision and management to identify opportunities to improve testing efficiencies</div></li><li><div>
Consistently communicates work sequence status to supervisor in a timely manner.</div></li><li><div>
Where scheduled work was not achieved, actively participates in discussions to identify opportunities for correction and improvement.</div></li><li><div>
Demonstrates engagement in helping to achieve CQ laboratory, team, and individual goals.</div></li><li><div>
When faced with roadblocks and issues, routinely offers suggestions for improvements and actively participates in associated improvement activities wherever possible</div></li><li><div>
Is a positive influence on the CQ laboratory, often going out of his/her way to support and assist teammates on the same shift and across shifts wherever possible.</div></li><li><div>
Maintains an on-time training</div></li><li><div>
Has understanding of basic non-instrumental wet chemistry techniques, Manual Titrations, pH, Conductivity, Autotitrations, UV-Vis, Polarimeter as wells as more advanced techniques, i.e. GC, HPLC, AA, FTIR, etc.</div></li></ul><div></div><div>
Here Is What You Need (Minimum Requirements)</div><ul><li><div>
A High School Diploma or GED with 4+ years of relevant experience</div></li><li><div>
Knowledge of laboratory equipment, testing, and techniques</div></li><li><div>
Basic math and computer skills, such as data entry</div></li><li><div>
High level of attention to detail</div></li><li><div>
Strong organizational skills</div></li><li><div>
Ability to multi-task across various projects and activities</div></li><li><div>
Self-motivated and able to work with minimal direction</div></li></ul><div></div><div>
Bonus Points If You Have (Preferred Requirements)</div><ul><li><div>
Proficiency in computerized systems such as Laboratory Information Management System</div></li><li><div>
Ability to train and support less experienced analysts</div></li><li><div>
Strong problem-solving skills</div></li><li><div>
Excellent communication skills</div></li></ul><div></div><div>
PHYSICAL/MENTAL REQUIREMENTS</div><div></div><div>
Stand up for up to 8 hours, sit for up to 8 hours, walking, climbing stairs, responding to visual warning indicators, respond to audible warning indicators, respond to color or special visual indicators, wear specialized protective clothing (lab coat, safety glasses, gloves, face shield/goggles, apron), repetitive use of upper extremities.</div><div></div><div>
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS</div><div></div><div>
1st shift position. Individual will be expected to work nonstandard schedule as needed to support the business objectives.</div><div><br>
Work Location Assignment: On Premise</div><div></div>
The salary for this position ranges from $22,94 to $38,24 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company&rsquo;s policies. 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 applies only to the United States - North Carolina - Rocky Mount location.<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></div></div></div></div></div><div></div>
Quality Assurance and Control<div></div>
#LI-PFE</div>

Job Id: tv+9OItdvKOrHBGKUICurxFjR4bPG1Ze2/0Xwnz8unGNM4KznbMuOPOF1ilcnwUBXfDVXGluXIMkLp6eie+FFWzOx5h27LjURoJ8lCxJ0xIFKv8DTuMfkeUyBGa0PMheIpMwVa4Hvd3yqXYYUXuHuzOzZVj3TOKHU8qnQt/toG0t4pHI9xZQrhZtAb00wweO3TNetY/Soz9qNqSWuW/wehM=

QC Lab Analyst II

<div><ul><li><div>Medical Science Liaison - Specialty Care.</div><div>
PURPOSE</div></li><li>
As a field-based (70-80% of the time) medical function, the Medical Scientific Liaison (MSL) provides scientific expertise, build knowledge and activity-based relationships with Key Opinion Leaders to advance medical practice and research for the benefit of the society, thus enhancing Pfizer&rsquo;s image in the scientific community across the Saudi markets. The MSL reports to the Specialty Care Medical Lead / Senior Medical Manager - Specialty Care.</li><li>
To actively contribute to the organization/business by taking responsibility for the scientific, technical and ethical soundness of all policies, statements and endeavors.</li><li>
To provide high quality and timely service in the areas of Interactions with Healthcare Professionals, Continuing Medical Education, Clinical Research, Sales Force Training, and business support in the areas of New Product Development, Regulatory Affairs, Quality Standards, and Business Technology.</li><li>
The role will act as a critical interface with identified scientific leaders and will build regional, national or international relationships to contribute to understanding of diseases, research and scientific trends, clinical practice guidelines, treatment patterns in areas relevant to our business.</li></ul><div></div><ul><li><div>
INTERACTIONS / ORGANIZATIONAL RELATIONSHIPS</div></li><li>
Internal (Marketing &ndash; Sales &ndash; Regulatory &ndash; Medical Information &ndash; legal-PHI)</li><li>
External (KOLs, Speakers, Decision Makers, Local Medical Societies, Health authorities)</li></ul><div></div><ul><li><div>
MAIN REPONSIBILITIES / DUTIES</div></li><li>
To provide medical and scientific information to healthcare professionals in response to their specific requests for Pfizer to present, orally or otherwise, clinical data about marketed products and important scientific information on new products, or those in development</li><li>
To liaise with healthcare professionals in order to effectively communicate and manage drug safety issues emanating from the region or of a national or international nature</li><li>
To develop and maintain medical and scientific partnerships with healthcare professionals</li><li>
To provide geographical focus and customer knowledge and insights, as members of Medical and Scientific Affairs team, to the development of the in-country clinical plan and to feed into above-country and global clinical plan (for marketed products as well as for those in development)</li></ul><div></div><ul><li><div>
Cross-Divisional Networks</div></li><li>
To develop and maintain ongoing cross-functional working relationships with Pfizer colleagues within the in-country and above country.</li></ul><ul><li><div>
REQUIRED SKILL SET</div></li><li>
University degree in Medicine or Pharmacy</li><li>
1-3 years&rsquo; corporate experience - preferably in specialized therapeutic areas.</li><li>
Inflammation and immunology experience are plus</li><li>
Saudi National is preferred.</li><li>
Excellent written and verbal communication skills.</li><li>
Excellent presentation skills.</li><li>
Project management skills.</li><li>
Excellent time management skills.</li><li>
Ability to both provide and receive constructive feedback.</li><li>
Build and maintain excellent relationships with colleagues and external customers.</li><li>
Proven self-starters, good planners and implementers, with experience of influencing others without authority and thinking analytically.</li></ul><br>
<div></div>
<br>
Work Location Assignment: On Premise<div></div><div><br>
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</div><div></div>
Medical<div></div>
#LI-PFE</div>

Job Id: fhKI4cu1PEN2hgC6gpebLzjmAinH2uwYi/VCp6GLZNrIbfohH45N56Rx9Omo5AtdWm1kLB4ZwowNgtrVRom7thaf4wjl5s7Tq2sfUZgPrPTzN3Hm3ODYdKUqXipB4qmIuZ4LrrCsHe6VAYKWcHQDKCcajA2KgpkxstQUEkD9FeTm4A6HKtS4Q9yCtcdfOKbUuoZIIj3DmU/IN1M1Gglp

Medical Science Liaison - Specialty Care

<div></div><div><div>Responsible for maximizing prod growth through the different sales &amp; promotion activities and being a business enabler through becoming a territory owner within certain geography.
</div><div>Key Activities:</div><ul><li>
Visiting physicians to promote Pfizer products</li><li>
Distributing product samples and marketing literature to HCP.</li><li>
Providing approved information to HCP on Pfizer products, e.g. proper medical usage, dosage amounts and side effects.</li><li>
Reporting visits and other activities using PforceRx.</li></ul><div>
Customer Relations:</div><ul><li>
Build relationships with target customers to enhance territory knowledge to gain product endorsement to generate sales.</li><li>
Ensure that accurate, timely and relevant customer knowledge is captured and shared with colleagues using agreed processes e.g. electronic customer management systems</li><li>
Segment and target high potential customers</li></ul><div>
Key Activities:</div><ul><li>
Visiting physicians with focus on target KOL and selected physicians in a given geography to promote Pfizer products and build strong relationship with them.</li><li>
Providing feedback to sales management on customer requests, responses to promotions and product access and competitive activities.</li></ul><div>
Territory Planning &amp; Management:</div><ul><li>
Diagnosis of situation of territory e.g., local market drivers and initiatives leading to subsequent design and implementation of territory action plan to achieve business objectives.</li><li>
Develop and execute territory business plan.</li></ul><div>
Key Activities:</div><ul><li>
Preparing POA for his/ her territory and products.</li><li>
Presenting reports according to HR Manager recommendations and market needs.</li><li>
Planning and organizing regular value-added programs.</li><li>
Organizing AV &amp; PHM activities.</li></ul><div>
Market Intelligence:</div><ul><li>
Feedback to Team, Head Office and Manager of relevant competitor activity or local issues to ensure appropriate action can be taken.</li></ul><div>
Key Activities:</div><ul><li>
Attending regular sales meetings with HRM, general meetings and cycle meetings.</li><li>
Capture and feedback on market intelligence</li></ul><div>
Teamwork:</div><ul><li>
Liaise with territory team members to share information, motivate and support team members and therefore contribute to the generation and delivery of the territory plan.</li></ul><div>
Key Activities:</div><ul><li>
Attend team meetings</li><li>
Share customer / territory information with colleagues</li></ul><div>
Administrative Systems:</div><ul><li>
Ensure territory and administrative systems/processes are maintained and updated to ensure an accurate record of territory is available at all times.</li></ul><div>
Key Activities:</div><ul><li>
Timely update of records and systems</li><li>
Produce reports - as requested by HRM</li><li>
Understand and work to SOPs</li></ul><div>
Self-Development:</div><ul><li>
Proactively implement/update personal development plans in order to develop self-further within current role</li></ul><div>
Key Activities.</div><ul><li>
Actively seek feedback</li><li>
Develop, own and implement IDP</li></ul><div>
Additional Assignments:</div><ul><li>
As agreed with line manager, undertake additional assignments, ensuring objectives are met and outputs delivered to the brief given</li></ul><div>
Criteria for applying:</div><ul><li>
Holding of bachelor's degree in pharmacy</li><li>
Young and dynamic</li><li>
Good command of English language, speaking, writing, listening and pronunciation</li><li>
Excellent knowledge of promoted products
</li><li>Knowledge of relevant therapeutic areas and competitors Effective selling and presentation skills</li><li>
Basic Computer ability - e.g., Excel / PowerPoint /Word/Outlook</li></ul><div><br>
<br>
Work Location Assignment: On Premise</div><div></div><div><br>
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</div><div></div>
Sales<div></div>
#LI-PFE</div>

Job Id: tkT6iwNdZScR8oZ0CNTR9QNF+U2IGNfalpyt7f7qG55D1KnFaRIaAtNoBB0n3ZVbDHvG61Vyrkkzqgymr+G86ivcNb9Vjrlez+7ZWoWCDv05suyQyZv4MwN34mHKMNspb9MPJbAwZEdyTaJeeiavXaN10eODDHG1DW0yLfdcvE+RHdM8no3Plf0LsKg=

Health Representative

Join Pfizer and explore 4 exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.