Manufacturing Associate II

ALLTECH CONSULTING SVC INC; Glen Burnie (MD); On-site; USD 10,000 - 60,000; Full time

Job summary

An established industry player is seeking a Manufacturing Associate II to support GMP upstream and downstream processes in the production of bulk biologics. This role involves completing Batch Production Records, generating operational protocols, and troubleshooting equipment issues. You'll collaborate with various teams to ensure compliance and efficiency in manufacturing operations. Ideal candidates will have a strong background in scientific principles, excellent documentation skills, and the ability to work effectively in a team environment. If you are passionate about biotechnology and looking to make a significant impact in a dynamic setting, this opportunity is perfect for you.

Qualifications

• 4-7 years of experience in biologic production processes under GMP compliance.
• Outstanding documentation skills and knowledge of cGMP.

Responsibilities

• Completes Batch Production Records and documents processes under cGMP.
• Troubleshoots process and equipment problems in manufacturing.

Skills

Scientific principles application

Documentation skills

Team-oriented collaboration

Communication skills

Education

High School or GED

Associate’s degree in Scientific, Engineering or Biotech

Bachelor’s degree in Scientific, Engineering or Biotech

Tools

Batch Production Records (BPR)

Standard Operating Procedures (SOP)

Job description

Job Description:

The Manufacturing Associate II is responsible for supporting the overall GMP upstream or downstream manufacturing process, through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk biologics from microbial and cell culture systems for Phase I/II & commercial GMP manufacturing.

• Lifting to 40 lbs., unassisted may be required at times.
• Frequent standing and walking is required, as this role requires presence on the manufacturing floor.
• Shift work and weekend work is required.

KEY RESPONSIBILITIES:

1. Completes Batch Production Records under cGMP, and documents in detail through the use of SOPs and BPRs for the processes and manufacturing steps.
2. Generates operational protocol(s), internal or external documents including SOPs, BPRs, deviations and summary reports.
3. May work with Process Development team and collaborate with Manufacturing Sciences and Technology group to transfer new projects into GMP.
4. Generate and revise internal and external documents (SOPs, BRs).
5. Support initiation and closure of deviations; may serve as the lead in the departmental investigation and be responsible for closing out deviations and CAPAs.
6. Troubleshoot process and equipment problems; Work with Facilities and Validation to maintain manufacturing equipment.
7. Recommend equipment and other supply purchases within the production areas.
8. Develop creative solutions to operational problems by leveraging knowledge of available theories and proven solutions.
9. Work closely with production management for current and new manufacturing projects and help develop processes/techniques to meet contract objectives and avoid operational delays.
10. Work closely with various departments and aid other teams as necessary.
11. Interact with clients during initial and subsequent manufacturing campaigns; may be responsible to oversee and escort the person-in-plant (PIP) during manufacturing campaigns.
12. Participate in facility expansion and equipment validation activities.
13. Is fully trained on all cGMP manufacturing operations and documentation and adhering to safety guidelines.
14. Other duties as assigned.

Education & Experience:

1. HS or GED with 4-7 years’ experience with upstream (fermentation/bioreactor) or downstream (column chromatography, buffer/media skid) biologic production processes under GMP compliance.
2. OR Associate’s degree in a Scientific, Engineering or Biotech field with 2-4 years’ experience with upstream (fermentation/bioreactor) or downstream (column chromatography, buffer/media skid) biologic production processes under GMP compliance.
3. OR Bachelor’s degree in a Scientific, Engineering or Biotech field with 1-3 years’ experience with upstream (fermentation/bioreactor) or downstream (column chromatography, buffer/media skid) biologic production processes under GMP compliance.

• Outstanding knowledge, and ability to apply scientific principles utilized to solve operational, as well as routine production tasks.
• Excellent documentation skills including comprehension, review & establishing Batch Production Records, SOP’s, deviation & summary reports.
• Thorough knowledge of current Good Manufacturing Practices (cGMP’s), and all relevant safety procedures within the company. General understanding of most areas in Manufacturing and supporting functional groups.
• Must be team-oriented (proactively builds healthy working relationships between peers, their department and other groups).
• Able to fluently communicate in English. Exhibits excellent written and oral communication skills.
• Possesses a basic knowledge of non-manufacturing functions such as QC, Regulatory, QA, and/or Materials Management.