Warehouse Specialist

Job Description

ONSITE - SHIFT - 7AM TO 7PM ON A 2-3-2 SCHEDULE. MUST ALSO BE ABLE TO WORK 7PM TO 7AM FOR TRAINING PURPOSES. DURATION - 3 + MONTHS AND MAY CONVERT TO FT FOR THE RIGHT EMPLOYEE.

The Central Services Technician I performs and documents cGMP activities related to Central Services production and operations. This involves operation of process equipment, execution of validation protocols, completion of cGMP documents, creating/ revising cGMP documents and other assignments as directed.

Shift work and/or weekend work may be required at times.

Key Responsibilities include but are not limited to:

• Performs Processing Steps and/or Manufacturing Support activities, monitoring process against the batch record.

• Documents/Records cGMP data and information for processing steps and/or equipment activities, following standard operating procedures. Key documentation includes batch records and equipment logbooks.

• Understands basic cGMP requirements and follows those requirements, including requirements for good documentation practices.

• Completes /reviews validation protocols, deviation reports, change controls in accordance with cGMP’s

• Performs the weighing, dispensing of raw materials for media and buffers

• Performs the preparation of small and large volume media and buffer solutions, filtration and transfer of product.

• Operates bench top equipment including pH, conductivity, osmo meters, pumps, tubing welders, filter integrity testers etc.

• Dispensing, labeling, transfer/staging of raw materials and parts

• Assembly/disassembly, cleaning and sterilization of components, parts and equipment

• Maintaining equipment, area and cleaning logbooks

• Cleaning sanitizing production rooms and equipment

• Stocking production and cleaning supplies

• May author/ review/improve SOP’s, batch records, protocols and technical reports

• Actively participates in training activities, managing their individual training plan.

• Proficient and knowledgeable in the operation and basic troubleshooting of at least one manufacturing area.

• Other duties as assigned

Education & Experience:

• High School Diploma with a minimum of 2-4 years GMP Manufacturing experience, OR

• Certificate and/or Associate’s Degree in a scientific, engineering or biotechnology discipline with a minimum of 0-2 years related experience; coursework with biotechnology focus highly desirable, OR

• Bachelor’s Degree (BS/BA) from an accredited college or university with an emphasis in a scientific or engineering discipline and a minimum of 0-1 years relevant experience

• Basic knowledge of current Good Manufacturing Practices (cGMP’s). Working knowledge of all relevant safety procedures within the company. General understanding of most areas in Manufacturing and supporting functional groups.

• Familiar with or experience with cGMP Biotech or Pharmaceutical operations:

• 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.Company Description

With almost four decades of experience as a proven industry leader, Acro continues to be consistently recognized among the Best & Brightest Companies to Work for in the United States. As an international professional services firm with deep expertise in consulting and staff augmentation offering a variety of solutions including MSP, VMS, RPO, HRO (and more), Acro operates across North America, Europe, and Asia from over 30 locations. Acro’s client portfolio includes some of the most well-known names in business and provides services across all verticals including technology, aerospace, energy, automotive, government, and manufacturing. To learn more, please visit