Job title: Manufacturing Associate
Contract on W2Â
Onsite from Severn MD 21077
Pay budget - $25 - $31/hr on W2
SHIFT - 7AM - 7PM
REQUIRED
•   The Manufacturing Associate I performs and documents cGMP activities to support upstream or downstream production areas and operations.Â
•   This involves the operation of process equipment, execution of validation protocols, completion of cGMP documents, creating/ revising cGMP documents and other assignments as directed.
•   Lifting to 40 LBS, unassisted may be required at times
•   Frequent standing and walking are required, as this role requires presence on the manufacturing floor.
•   Shift work and weekend work are required.
EDUCATION & EXPERIENCE
•   High School Diploma with a minimum of 2-4 years GMP Manufacturing experience, OR
•   Associate’s degree in a scientific, engineering or biotechnology discipline with a minimum of 1-2 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 scientific or engineering discipline and some relevant work experience
•   Basic knowledge of current Good Manufacturing Practices (cGMPs). 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.
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 cGMPs
•   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 SOPs, 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
Back to searchManufacturing Associate
Manpower Engineering
Posted a day ago, valid for 6 months
Harmans, MD 21077, US
$35,000 - $42,000 per annum
Part Time
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Sonic Summary
- The Manufacturing Associate position is a contract role located onsite in Severn, MD, offering a pay range of $25 to $31 per hour on W2.
- Candidates are required to have a High School Diploma with 2-4 years of GMP Manufacturing experience, or an Associate's degree with 1-2 years of related experience, or a Bachelor's degree with some relevant work experience.
- The role involves performing and documenting cGMP activities, operating process equipment, and ensuring compliance with safety and documentation standards.
- Physical requirements include lifting up to 40 lbs, frequent standing and walking, and the need for shift and weekend work.
- Strong communication skills and the ability to work collaboratively in a team-oriented environment are essential for this position.
