Biopharmaceutical Manufacturing Specialist

TapTalent.ai; Philadelphia (Philadelphia County); On-site; USD 55,000 - 70,000; Full time

Job summary

A leading company in Philadelphia is seeking a detail-oriented Biopharmaceutical Manufacturing Specialist to oversee the manufacturing process. The ideal candidate will ensure compliance with regulatory standards and collaborate with teams to enhance production efficiency. This entry-level role offers a full-time position in a dynamic environment focused on quality assurance in biopharmaceutical production.

Qualifications

• At least 2 years of experience in biopharmaceutical manufacturing or similar role.
• Strong understanding of cGMP regulations and quality management systems.

Responsibilities

• Oversee the biopharmaceutical manufacturing process from start to finish.
• Ensure compliance with all regulatory standards and company policies.
• Conduct batch record reviews and product testing for quality assurance.

Skills

Problem Solving

Attention to Detail

Education

Bachelor’s degree in Life Sciences

Job description

Biopharmaceutical Manufacturing Specialist

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Position Overview

We are seeking a detail-oriented and skilled Biopharmaceutical Manufacturing Specialist to join our team in Philadelphia. The ideal candidate will have experience in biopharmaceutical production processes, quality assurance, and regulatory compliance to ensure the safe and efficient manufacture of biopharmaceutical products.

Location and Work Mode

Location: Philadelphia, United States

Work Mode: Work From Office

Responsibilities

• Oversee the biopharmaceutical manufacturing process from start to finish.
• Ensure compliance with all regulatory standards and company policies.
• Perform routine equipment maintenance and troubleshooting as needed.
• Conduct batch record reviews and product testing for quality assurance.
• Collaborate with cross-functional teams to improve manufacturing processes.
• Maintain accurate documentation of production activities and results.

Qualifications

• Bachelor’s degree in Life Sciences or related field.
• At least 2 years of experience in biopharmaceutical manufacturing or similar role.
• Strong understanding of cGMP regulations and quality management systems.
• Excellent problem-solving skills and attention to detail.
• Ability to work effectively in a team-oriented environment.

Additional Information

Seniority level: Entry level

Employment type: Full-time

Job function: Other

Industries: IT Services and IT Consulting

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