Manufacturing Associate

Abacus Service Corporation; Harmans (MD); On-site; USD 37,000 - 55,000; Full time

Job summary

A leading biotechnology company is seeking a Manufacturing Associate I to support cGMP activities in their production area. The role involves operating process equipment, documenting activities, and adhering to safety standards. A background in sciences or relevant manufacturing experience is preferred for candidates looking to thrive in a hands-on environment.

Qualifications

• Experience in GMP manufacturing preferred.
• Familiarity with biotech or pharmaceutical operations.
• Basic understanding of QC, Regulatory, QA, and Materials Management.

Responsibilities

• Perform processing steps and support activities monitoring against batch records.
• Document cGMP data; understand and adhere to good documentation practices.
• Operate bench top equipment and maintain equipment logbooks.

Skills

Communication skills

Team-oriented

Basic knowledge of cGMPs

Education

High School Diploma

Associate's Degree in a scientific, engineering, or biotech discipline

Bachelor's Degree in a scientific or engineering field

Tools

pH meters

Conductivity meters

Pumps

Welders

Testers

Job description

Description / Comment : - SHIFT - PM - AM (ROTATION) - ONSITE POSITION - DURATION - X MONTHS

The Manufacturing Associate I performs and documents cGMP activities to support upstream or downstream production areas and operations. Responsibilities include operation of process equipment, execution of validation protocols, and creation/revision of cGMP documents.

Physical Requirements: Lifting to lbs., unassisted may be required at times. Frequent standing and walking are required on the manufacturing floor.

Key Responsibilities include but are not limited to :

• Perform processing steps and support activities, monitoring processes against batch records.
• Document cGMP data, including batch records and equipment logs, following SOPs.
• Understand and adhere to cGMP requirements and good documentation practices.
• Complete/review validation protocols, deviation reports, change controls.
• Weighing, dispensing raw materials, preparing media and buffer solutions, filtration, and transfer of product.
• Operate bench top equipment like pH meters, conductivity meters, pumps, welders, and testers.
• Handle raw materials and parts: dispensing, labeling, transfer, staging.
• Assemble/disassemble, clean, and sterilize components and equipment.
• Maintain equipment and area logbooks, clean and sanitize production rooms and equipment.
• Stock supplies, and potentially author/review SOPs, batch records, protocols, and reports.
• Participate in training activities and manage individual training plans.
• Proficient in operation and troubleshooting of at least one manufacturing area.
• Perform other duties as assigned.

Education & Experience :

• High School Diploma with GMP manufacturing experience of X years, OR
• Associate's Degree in a scientific, engineering, or biotech discipline with X years of related experience, preferably with biotech coursework, OR
• Bachelor's Degree in a scientific or engineering field with relevant experience.

Knowledge and Skills:

• Basic knowledge of cGMPs and safety procedures.
• Familiarity with biotech or pharmaceutical manufacturing operations.
• Team-oriented with strong communication skills in English.
• Basic understanding of QC, Regulatory, QA, and Materials Management functions.

Physical Demands :

• Extended walking, standing, bending, reaching, pushing, and pulling.

Start Time : AM hours. Location : Harmans Rd., Harmans, MD, United States.