13 days old

Tech Associate, Clinical Manufacturing, Upstream

Pfizer
Andover, MA 01810
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**ROLE SUMMARY**

At Pfizer, we innovate every day to make the world a healthier place. It was the vision of Charles Pfizer at the very beginning and it holds true today in everything we do. From scientific discovery to breakthrough products to our essential partnerships around the world, we're committed to quality healthcare for everyone. Because every individual matter. Our medicines and vaccines save or improve countless lives and our consumer products empower people to take care of themselves. Pfizer Corporate Responsibility believes that all individuals, everywhere, deserve access to quality healthcare and the opportunity to lead healthy lives.



Diversity, equality and inclusion are an integral component of Pfizer's mission to build a vibrant culture. We maintain the highest standards of ethics and compliance in all of our business practices.



The clinical manufacturing Technical Associate is part of a multi-disciplinary team responsible for cGMP production of phase I/II clinical drug substance supporting the Pfizer Biotherapeutics portfolio.



The successful candidate will be a part of the cell culture team responsible for the execution of mammalian and microbial processes. The successful candidate will have the opportunity to work with both Single-Use Technology (i.e Single Use Bioreactors) and Stainless-Steel Bioreactors to manufacture Phase I/II clinical drug substance.

This is a 1st Shift position (M-F, 7:00AM-3:30PM).



**ROLE RESPONSIBILITIES**



+ Execute upstream mammalian cell culture and microbial fermentation processes in a cGMP environment. Includes CIP and SIP operations.

+ Execute product change over activities with the guidance of process engineer and tech transfer team.

+ Execution of SOP's and batch record documentation of upstream unit operations.

+ Cross-functional communication with tech transfer team, quality and engineering as necessary.

+ Cross-shift communication with 2st shift. Actively participates in shift exchange activities and communication channels.

+ Active participant of the OWN IT culture. Identifies and supports continuous improvement initiatives. Utilizes continuous improvement and root cause analysis tools ( 5S and DMAIC)

+ Maintains a safe work environment.

+ Effectively uses process automation systems (i.e. Delta V and OSI/Pi Historian) and supporting business systems (i.e. Microsoft Dynamics/SAP/ERP Systems, Trackwise, Document Management Systems, Microsoft Sharepoint etc.)



**BASIC QUALIFICATIONS**



+ HS diploma, Associates Degree, or BS/BA in Biotechnology, Microbiology, Cell Biology, Chemical Engineering, Biochemistry or equivalent.

+ Requires a minimum 0-3 years of experience in a biotechnology manufacturing or laboratory environment.



**PREFERRED QUALIFICATIONS**



+ Prior experience in a Biological Pilot Plant, cGMP Clinical or Commercial Manufacturing setting.

+ Knowledge of mammalian cell culture and/or microbial fermentation processes.

+ Familiarity with Production Control Systems (i.e. DeltaV), ERP Systems (i.e. Microsoft Dynamics and/or SAP) and other business systems (Document Management Systems, LIMS, Microsoft Word, Excel, etc.)

+ Ability to follow Standard Operating Procedures and work under minimal supervision.

+ Fundamental mechanical aptitude and ability to interface with computerized systems required.

+ Demonstrated capability to work as a team member in a matrix manufacturing team.

+ Excellent oral and written communication skills.



**ADDITIONAL INFORMATION**



+ Eligible for Employee Referral Bonus: Yes

+ **Last Date to Apply: April 15, 2020**

+ \#LI-PFE



**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: 2020-03-16 Expires: 2020-04-16

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Tech Associate, Clinical Manufacturing, Upstream

Pfizer
Andover, MA 01810

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