Job Title: Downstream Processing SupervisorJob Description

The Downstream Processing Supervisor is accountable for the success and oversight of downstream manufacturing processes, with responsibilities that encompass large scale chromatography, viral inactivation, viral filtration, ultrafiltration, diafiltration, and aseptic filling of bulk drug substances.

ResponsibilitiesExecute manufacturing batch records, work instructions, and SOPs with a focus on 'right the first time' executions, and assist with batch record reconciliation.Complete all department functions such as maintaining suite, supplies, equipment, logbooks, and data in accordance with site SOPs and policies.Document all activities to meet cGMP requirements, including daily record review, tasks, and databases.Forecast and resolve supply and raw material deficiencies, and identify and resolve scheduling conflicts with a one-week outlook.Identify deviations, aid in investigations/root cause analysis, and provide input on major/critical deviations.Represent the manufacturing team at tier meetings and promote safe work habits by adhering to safety procedures and guidelines.Utilize manufacturing process knowledge and investigational skills to identify and resolve manufacturing issues, driving continuous improvement in process operations.Provide feedback on document revisions and/or management including batch production records and manufacturing procedures.Maintain a safe and clean work environment by educating and directing personnel to ensure compliance with established policies and procedures.Coordinate training with team either in class or on the floor, as needed, and help build cross-functional relationships.Provide frequent feedback and coaching to others to improve performance.Complete the production plan by scheduling and assigning personnel, prioritizing tasks, supervising progress, revising schedules, resolving problems, and reporting results.Lead shift exchanges and daily huddles for the team as required, act as liaison with other groups within the manufacturing organization, and be a Subject Matter Expert on various techniques.Essential Skills5-9 years of experience working in cGMP manufacturing with a high school diploma or GED; Bachelor's degree preferred.2+ years of supervisory and leadership experience in a pharmaceutical manufacturing setting.Experience in a cGMP environment and knowledge of cGMP practices.Strong math skills, aseptic techniques, and chemical concepts.Critical thinking and problem-solving capabilities.Detail-oriented and results-driven.Proficiency in MS Office.Additional Skills & QualificationsExperience with bioreactor, chromatography, purification, and Lean manufacturing.Familiarity with cleanroom and aseptic techniques.Work Environment

The work environment includes cleanroom and aseptic suites where full gowning is required, including bodysuit, gloves, hair and beard nets, face covers, and safety glasses. The role involves night shifts from 6:15 pm to 6:45 am with rotating 12-hour shifts, working 7 days out of a 2-week period. The position requires the ability to lift a minimum of 25 lbs independently and the ability to stand for 80% of the shift.

Job Type & Location

This is a Contract to Hire position based out of Saint Louis, MO.

Pay and Benefits

The pay range for this position is $43.00 - $48.00/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: \u2022 Medical, dental & vision \u2022 Critical Illness, Accident, and Hospital \u2022 401(k) Retirement Plan \u2013 Pre-tax and Roth post-tax contributions available \u2022 Life Insurance (Voluntary Life & AD&D for the employee and dependents) \u2022 Short and long-term disability \u2022 Health Spending Account (HSA) \u2022 Transportation benefits \u2022 Employee Assistance Program \u2022 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 Feb 19, 2026.

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 actalentaccommodation@actalentservices.com for other accommodation options.