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Bioprocessing Upstream Manager Jobs (NOW HIRING)

The successful candidate will have a demonstrated background in bioprocessing (upstream and/or ... matrix management environments, as well as independent working environments to support the site.

Manufacturing Supervisor - Aseptic Upstream Bioprocessing** is responsible for leading ... Supervise, coach, and develop manufacturing personnel through performance management, training, and ...

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... upstream processing equipment. Specific Duties Include: * Serve as a valuable member of the ... Provide timely and accurate verbal and written communication to team members and management. * Work ...

Be Seen First

... upstream processing equipment. Specific Duties Include: * Serve as a valuable member of the ... Provide timely and accurate verbal and written communication to team members and management. * Work ...

Be Seen First

... upstream processing equipment. Specific Duties Include: * Serve as a valuable member of the ... Provide timely and accurate verbal and written communication to team members and management. * Work ...

Be Seen First

... upstream processing equipment. Specific Duties Include: * Serve as a valuable member of the ... Provide timely and accurate verbal and written communication to team members and management. * Work ...

$135K - $200K/yr

We're united by a mission to inspire advances in bioprocessing as a preferred partner in the ... This role will lead the upstream filtration products including ATF and TFDF systems used for ...

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Bioprocessing Upstream Manager information

What are popular job titles related to Bioprocessing Upstream Manager jobs?

For Bioprocessing Upstream Manager jobs, the most frequently searched job titles are:

Process Engineer - Upstream/Downstream

Devens, MA

Integrated Resources INC
Recruiting and Staffing Services • 51 - 200 employees

Contractor

Re-posted 22 days ago


Job description

Company Description

Client is a global bio-pharmaceutical company

Job Description

The successful candidate will provide meaningful contributions toward commercial manufacturing support, process monitoring, technology transfer and process validation activities. The successful candidate will have a demonstrated background in bioprocessing (upstream and/or downstream), experience troubleshooting manufacturing processes and strong technical documentation skills (memos, protocols, reports).

Responsibilities:

Work independently to provide commercial manufacturing technical support, process monitoring, technology transfer and process validation activities for downstream processes.

Provide process troubleshooting during scale-up and routine manufacturing.

Provide process subject matter expertise and ownership of assigned deliverables.

The successful candidate will work effectively in highly cross-functional project teams, matrix management environments, as well as independent working environments to support the site.

Perform data analysis and monitoring for process performance and product quality outputs.

The position will interface with Manufacturing, Quality, Engineering, and internal MS&T departments at multiple sites throughout the Client network

Strong communication and technical writing skills are required.

Qualifications

B.S./M.S. or Ph.D. in Chemical Engineer, Biochemical Engineer, Biomedical Engineer, Biochemistry or related field (Advanced degree is preferred)

Required: Prior experience (Ph.D: 0 - 2 years; BS/MS: 2 - 6 years) in process development, process validation or manufacturing support in bioprocessing (upstream and/or downstream)

Preferred: Prior experience scaling up biopharma manufacturing processes (upstream/downstream), facility fit assessments, process scale-up from bench/pilot to production, process troubleshooting and optimization, and process validation.

Hands-on experience working with chromatography, ultrafiltration and depth filtration process acquired through lab, pilot or production scale experience.

Preferred: Experience performing manufacturing investigations for biologics manufacturing.

Preferred: Experience providing start-up support for new biologics manufacturing processes (Person-In-Plant)

Preferred: Experience with statistical methodologies (DOE, SPC, etc), cGMP regulations, and regulatory requirements is expected.

Additional Information

All your information will be kept confidential according to EEO guidelines.


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About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996