22 days old

Manager, Drug Product Manufacturing

Pfizer
Andover, MA 01810
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**Why Patients Need You**



Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members, who understand the importance and impact of their role in Pfizer's mission. Patients need colleagues like you who take pride in their work and always look to improve outcomes. You will help to ensure that patients and physicians have the medicines they need, when they need them.



This position is part of t he Biotherapeutics PhRD Clinical Manufacturing Technical Services Group and is responsible for management of sterile clinical drug product manufacturing and technology transfer for internal Pfizer and external Contract Manufacturing Organizations (CMOs). The position may be located in Andover, MA, Chesterfield, MO, Chapel Hill, NC or Cambridge, UK and will directly interface with manufacturing sites, Drug Product Design and Development (DPDD) groups within PhRD, QA, Analytical, Project Teams and Global Clinical Supplies (GCS).



**Role Responsibilities**



+ The Tech Services Leads (TSL) manage technology transfer for BioTherapeutics clinical sterile drug product manufacturing.

+ Manage Phase I and II sterile vial and pre-filled syringe drug product clinical manufacturing at multiple Contract Manufacturing Organizations (CMOs).

+ Manage and support Phase III and commercial launch sterile drug product manufacturing at Pfizer commercial sites in the US and Europe.

+ Develop, review and approve technology transfer documents for manufacturing of clinical and commercial supplies.

+ Oversee efforts and closely work with CMOs, QA, Analytical, Formulation and Supply Chain organizations to ensure timely manufacture and delivery of clinical supplies for parenteral drug products.

+ Lead quality investigations and develop and implement agreed upon corrective and preventative actions.

+ Represent Tech Services group on site during engineering trials and clinical manufacturing of drug product supplies at CMOs and Pfizer PGS sites.

+ Liaise with formulation and process development groups to manage development of new drug product manufacturing processes for internal and external manufacturing sites.

+ Lead manufacturing team discussions to ensure manufacturing readiness to meet clinical supply needs based on agreed schedules. Review and approve manufacturing batch records to ensure compliance with cGMP requirements.



**Qualifications**



+ Bachelor's degree in a scientific discipline, preferred fields include Life Science or Engineering

+ Minimum of 5 years of direct experience in GMP manufacture or sterile drug product development or manufacturing. Training in cGMP compliance, parenteral process technology and knowledge of regulatory requirements for sterile drug product manufacturing is preferred.



**NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS**



+ About 10 % domestic and international travel will be required in support of manufacturing activities at CMOs or Pfizer Global Supply sites.



**Additional Job Information**



+ Eligible for Employee Referral Program



**Sunshine Act**



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'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.



**EEO & Employment Eligibility**



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.



Manufacturing
Posted: 2021-05-21 Expires: 2021-06-28
Sponsored by:
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Manager, Drug Product Manufacturing

Pfizer
Andover, MA 01810

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