Bioprocess Engineer
Huntsville, AL · On-site
Company Description A fully integrated biopharmaceutical company focused on developing a portfolio ... The position will play an integral role in the establishment of a GMP manufacturing facility to ...
Bioprocess Engineer
Huntsville, AL · On-site
Company Description A fully integrated biopharmaceutical company focused on developing a portfolio ... The position will play an integral role in the establishment of a GMP manufacturing facility to ...
Bioprocess Engineer
Huntsville, AL · On-site
Company Description A fully integrated biopharmaceutical company focused on developing a portfolio ... The position will play an integral role in the establishment of a GMP manufacturing facility to ...
Bioprocess Engineer
Huntsville, AL · On-site
Company Description A fully integrated biopharmaceutical company focused on developing a portfolio ... The position will play an integral role in the establishment of a GMP manufacturing facility to ...
CSL Plasma is a subsidiary of CSL, a global biopharma company. Plasma collected at CSL Plasma facilities is used by CSL for the sole purpose of manufacturing lifesaving plasma-derived therapies for ...
CSL Plasma is a subsidiary of CSL, a global biopharma company. Plasma collected at CSL Plasma facilities is used by CSL for the sole purpose of manufacturing lifesaving plasma-derived therapies for ...
Whether you are involved in manufacturing, testing, or compliance, your contribution will directly ... Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who ...
Whether you are involved in manufacturing, testing, or compliance, your contribution will directly ... Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who ...
Biopharmaceutical Manufacturing Associate information
See Alabama salary details
$16.78 - $18.56
4% of jobs
$18.56 - $20.34
6% of jobs
$20.93 is the 25th percentile. Wages below this are outliers.
$20.34 - $22.13
44% of jobs
$22.13 - $23.91
9% of jobs
$23.91 - $25.69
3% of jobs
$25.69 - $27.47
1% of jobs
$28.22 is the 75th percentile. Wages above this are outliers.
$27.47 - $29.26
16% of jobs
$29.26 - $31.04
15% of jobs
$31.04 - $32.82
0% of jobs
$32.82 - $34.60
0% of jobs
$34.60 - $36.39
1% of jobs
$16
$24
$36
How much do biopharmaceutical manufacturing associate jobs pay per hour?
As of Sep 3, 2026, the average hourly pay for biopharmaceutical manufacturing associate in Alabama is $24.58, according to ZipRecruiter salary data. Most workers in this role earn between $20.91 and $28.75 per hour, depending on experience, location, and employer.
What is a biopharmaceutical manufacturing associate?
As a biopharmaceutical manufacturing associate, your primary responsibilities are to prepare equipment and materials for the production of biopharmaceutical products. Your duties include moving the product, supplies, and inventory to support the manufacturing process and operating devices like autoclaves and washers. You monitor the production and operations, make adjustments to increase efficiency, and ensure that you are meeting all safety regulations. You work with downstream and upstream processes to control quality. You are also in charge of preparing reports and reviewing GMP documents to ensure compliance with laws and industry regulations.
What does a biopharmaceutical manufacturing associate do?
A Biopharmaceutical Manufacturing Associate is responsible for producing biopharmaceutical products such as vaccines, antibodies, or therapeutic proteins under strict regulatory guidelines. Their tasks typically include preparing equipment, monitoring production processes, maintaining sterile environments, and ensuring that all procedures adhere to Good Manufacturing Practices (GMP). They may also be involved in quality control, documentation, and troubleshooting equipment issues. This role is crucial for ensuring the safety, efficacy, and quality of biopharmaceutical products.
What are the key skills and qualifications needed to thrive as a biopharmaceutical manufacturing associate?
To thrive as a Biopharmaceutical Manufacturing Associate, you need a solid background in life sciences or engineering, with knowledge of GMP (Good Manufacturing Practices) and often a relevant bachelor’s degree or associate’s certification. Familiarity with bioprocessing equipment, automation systems like SCADA, and quality control tools is essential. Attention to detail, teamwork, and strong communication skills are crucial soft skills for this role. These competencies ensure the safe, accurate, and compliant production of high-quality biopharmaceutical products.
What are some common challenges faced by biopharmaceutical manufacturing associates, and how can they be addressed?
Biopharmaceutical Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP) and troubleshooting equipment malfunctions under tight production schedules. To address these challenges, associates are trained extensively on standard operating procedures and cross-functional communication to quickly resolve issues. Teamwork and attention to detail are essential, as the role frequently involves collaborating with quality assurance, engineering, and process development teams to ensure product safety and compliance. Continuous learning and proactive problem-solving are key to success in this dynamic environment.
What is the difference between Biopharmaceutical Manufacturing Associate vs Quality Control Technician?
| Aspect | Biopharmaceutical Manufacturing Associate | Quality Control Technician |
|---|---|---|
| Primary Role | Supports production processes, prepares materials, and ensures manufacturing runs smoothly | Performs testing and inspection of products to ensure quality standards |
| Required Skills | Knowledge of GMP, aseptic techniques, and manufacturing procedures | Laboratory skills, attention to detail, knowledge of testing methods |
| Work Environment | Cleanrooms, manufacturing floors, production facilities | Laboratories, testing labs, quality control areas |
| Certifications | GMP training, sometimes cGMP certification | Lab safety, GMP, and quality assurance training |
The Biopharmaceutical Manufacturing Associate focuses on supporting the production process in manufacturing environments, while the Quality Control Technician specializes in testing and verifying product quality. Both roles require GMP knowledge and work in regulated settings, but their daily tasks and skill sets differ significantly.
More about Biopharmaceutical Manufacturing Associate jobs
What are popular job titles related to Biopharmaceutical Manufacturing Associate jobs in Alabama?
For Biopharmaceutical Manufacturing Associate jobs in Alabama, the most frequently searched job titles are:
What job categories do people searching Biopharmaceutical Manufacturing Associate jobs in Alabama look for?
The top searched job categories for Biopharmaceutical Manufacturing Associate jobs in Alabama are:
What cities in Alabama are hiring for Biopharmaceutical Manufacturing Associate jobs?
Cities in Alabama with the most Biopharmaceutical Manufacturing Associate job openings:
Full-time
Re-posted 25 days ago
Job description
Company Description
A fully integrated biopharmaceutical company focused on developing a portfolio of innovative treatments for cancer and infectious diseases using their DNA-mediated gene transfer technologies.
Job Description
Company is seeking to hire a Bioprocess Engineer to support the company's ongoing development of novel immunotherapies. The position will play an integral role in the establishment of a GMP manufacturing facility to produce plasmid DNA active pharmaceutical ingredient (API).
• Lead the development of pilot scale downstream processing (DSP) unit operations of plasmid DNA from bacterial cell paste (from 10 L - 100 L bioreactor fermentation), to include lysis, clarification, ultrafiltration/diafiltration, and ion exchange chromatography.
• Plan and execute structured process development experiments to achieve the target yield, process optimization, product quality, scale-up and process robustness objectives.
• Play a pivotal role in the establishment of a GMP manufacturing facility to produce plasmid DNA active pharmaceutical ingredient (API).
• Document work thoroughly with a detail-oriented approach, write concise technical reports, and make effective presentations to management and other team members.
• Translate developed processes into standard operating procedures (SOPs) as well as necessary calibration and preventive maintenance SOPs.
• Write validation protocols and lead the technical support staff to successfully execute IQ, OQ, and PQ.
• Lead the process transition into the new facility.
• Troubleshoot, optimize, and improve ongoing process activity with scientific curiosity.
Qualifications
• B.S. or M.S. degree in Biochemical/Chemical Engineering preferred. Will also consider other disciplines such as biology, chemistry, or related field with requisite experience.
• 4+ years of hands-on biopharmaceutical experience at pilot or commercial scale with bioreactor fermentation (USP) and DSP of plasmid DNA from bacterial cell paste, including lysis, clarification, ultrafiltration/diafiltration, and ion exchange chromatography.
• 2+ years of experience working in a GMP manufacturing environment. Candidates with supervisory experience are preferred.
• Significant experience using ultrafiltration and diafiltration with tangential flow filtration (TFF) in a DSP unit operation.
Additional Information
Competitive salary, bonus, stock, relocation and benefits are offered.
A fully integrated biopharmaceutical company focused on developing a portfolio of innovative treatments for cancer and infectious diseases using their DNA-mediated gene transfer technologies.
Job Description
Company is seeking to hire a Bioprocess Engineer to support the company's ongoing development of novel immunotherapies. The position will play an integral role in the establishment of a GMP manufacturing facility to produce plasmid DNA active pharmaceutical ingredient (API).
• Lead the development of pilot scale downstream processing (DSP) unit operations of plasmid DNA from bacterial cell paste (from 10 L - 100 L bioreactor fermentation), to include lysis, clarification, ultrafiltration/diafiltration, and ion exchange chromatography.
• Plan and execute structured process development experiments to achieve the target yield, process optimization, product quality, scale-up and process robustness objectives.
• Play a pivotal role in the establishment of a GMP manufacturing facility to produce plasmid DNA active pharmaceutical ingredient (API).
• Document work thoroughly with a detail-oriented approach, write concise technical reports, and make effective presentations to management and other team members.
• Translate developed processes into standard operating procedures (SOPs) as well as necessary calibration and preventive maintenance SOPs.
• Write validation protocols and lead the technical support staff to successfully execute IQ, OQ, and PQ.
• Lead the process transition into the new facility.
• Troubleshoot, optimize, and improve ongoing process activity with scientific curiosity.
Qualifications
• B.S. or M.S. degree in Biochemical/Chemical Engineering preferred. Will also consider other disciplines such as biology, chemistry, or related field with requisite experience.
• 4+ years of hands-on biopharmaceutical experience at pilot or commercial scale with bioreactor fermentation (USP) and DSP of plasmid DNA from bacterial cell paste, including lysis, clarification, ultrafiltration/diafiltration, and ion exchange chromatography.
• 2+ years of experience working in a GMP manufacturing environment. Candidates with supervisory experience are preferred.
• Significant experience using ultrafiltration and diafiltration with tangential flow filtration (TFF) in a DSP unit operation.
Additional Information
Competitive salary, bonus, stock, relocation and benefits are offered.
About Phil Ellis Associates
Sourced by ZipRecruiter
Industry
Recruiting and staffing services
Company size
11 - 50 Employees
Headquarters location
Wrightsville Beach, NC, US
Year founded
1978