What are the responsibilities and job description for the GMP Manufacturing Support Specialist position at Acro Service Corp?
Production Team Member:
We are seeking a highly skilled GMP Manufacturing Support Specialist to join our production team. As a key member of our team, you will be responsible for performing and documenting cGMP activities to support upstream or downstream production areas and operations.
This role offers the opportunity to develop your skills in process equipment operation, validation protocols, and document creation. You will work closely with our experienced production team to ensure compliance with cGMP regulations and standards.
Responsibilities and Requirements:
We are seeking a highly skilled GMP Manufacturing Support Specialist to join our production team. As a key member of our team, you will be responsible for performing and documenting cGMP activities to support upstream or downstream production areas and operations.
This role offers the opportunity to develop your skills in process equipment operation, validation protocols, and document creation. You will work closely with our experienced production team to ensure compliance with cGMP regulations and standards.
Responsibilities and Requirements:
- 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;
- Basic knowledge of current Good Manufacturing Practices (cGMP's).
- Working knowledge of all relevant safety procedures within the company.
- Familiar with or experience with cGMP Biotech or Pharmaceutical operations.
- Able to fluently communicate in English.
- Exhibits excellent written and oral communication skills.
