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Sr. Biopharmaceutical Processing Technician

Job Description

In this role, you will support the performance of operations in the manufacture of Commercial and Clinical Biologics, adhering to Current Good Manufacturing Practices (cGMPs). Your responsibilities will include executing manufacturing batch records and maintaining a high standard of compliance and safety. You will be part of a dynamic team, ensuring all tasks are completed accurately and contributing to process improvement initiatives.

Responsibilities

+ Execute manufacturing batch records, work instructions, and SOPs with a focus on 'right the first time' executions.

+ Assist with batch record reconciliation and maintain suite, supplies, equipment, logbooks, and data according to cGMP standards.

+ Document all activities to meet cGMP requirements and complete document reviews and revisions.

+ Participate in shift exchanges, meetings, and lean activities to facilitate area needs.

+ Support quality investigations by providing feedback and suggesting improvements.

+ Practice and promote safe work habits, adhering to safety procedures and guidelines.

+ Critically evaluate processes, prioritize tasks, and complete them according to production schedules.

+ Manufacture buffers and simple bulk reagents per manufacturing procedures with limited supervision.

+ Review area documents and assist in the manufacture of controls and calibrators, completing batch records following cGMPs.

+ Perform in-process assays using equipment such as spectrophotometers, pH meters, and clinical analyzers.

+ Weigh, transfer, and mix chemicals as required and perform product filtrations.

+ Clean and steam steel tanks (CIP/SIP) and prepare glassware and steel tanks for sterilization in an autoclave.

+ Maintain lab equipment, monitor lab supplies, and respond to emergency notifications.

+ Perform other job duties as required and be flexible with work hours, including weekends.

Essential Skills

+ Bachelor's Degree in Science with experience in aseptic technique, cell culturing, pipetting, chromatography, and biochemistry.

+ Minimum of 2 years of work experience in manufacturing, operation, production, lab setting, or related field.

+ Knowledge of cGMP practices, aseptic techniques, and chemical concepts.

Additional Skills & Qualifications

+ Experience in a cGMP environment preferred.

+ Subject Matter Expert on upstream processing steps preferred.

+ Preferred experience of 6 months in a GMP regulated environment.

Work Environment

The work environment includes cleanroom/aseptic suites, requiring full gowning, including bodysuit, gloves, and safety gear. Shifts are rotating 12-hour days, working 7 days out of a 2-week period. Employees must be able to lift a minimum of 25 lbs independently and stand for 80% of their shift.

Pay and Benefits

The pay range for this position is $28.00 - $28.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Saint Louis,MO.

Application Deadline

This position is anticipated to close on Oct 27, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.