Executive/Sr. Executive/Asst. Manager - Manufacturing

Intas; Ahmedabad District; On-site; INR 600,000 - 1,100,000; Full time

Job summary

Intas in Ahmedabad seeks an experienced bioprocess specialist to manage upstream and downstream manufacturing steps, ensuring GMP compliance and high product quality. You will collaborate with cross-functional teams to optimize processes, reduce costs, and implement strategies to improve yield while maintaining strict batch records and regulatory adherence.

The role requires proficiency in cell culture, purification, chromatography, filtration, and contamination control, with a strong focus on

Qualifications

• Experience in biopharmaceutical manufacturing environments.
• Knowledge of GMP/cGMP requirements and regulatory expectations.
• Ability to manage upstream and downstream processing steps with emphasis on quality and yield.

Responsibilities

• Manage upstream processing operations, including cell culture, filtration, and sterilization.
• Oversee downstream processing activities such as purification and concentration of biopharmaceuticals.
• Ensure compliance with cGMP regulations and maintain accurate records of production batches.
• Collaborate with cross-functional teams to optimize process efficiency and reduce costs.
• Develop and implement strategies to enhance product quality and yield.
• Monitor and control processes to prevent contamination or defects.
• Experience in microbial processing, downstream processing, mammalian cell culture, and upstream processing.
• Strong understanding of downstream processing techniques including filtration, centrifugation, and chromatography.
• Experience working in a regulated environment (cGMP).
• Familiarity with quality control measures and regulatory requirements.

Skills

Cell culture

Filtration

Sterilization

Downstream processing

Purification

Concentration

cGMP compliance

Batch records

Process optimization

Cost reduction

Cross-functional collaboration

Product quality improvement

Process monitoring

Contamination prevention

Quality control

Regulatory familiarity

Problem-solving

Attention to detail

Job description

• Manage upstream processing operations, including cell culture, filtration, and sterilization.
• Oversee downstream processing activities such as purification and concentration of biopharmaceuticals.
• Ensure compliance with cGMP regulations and maintain accurate records of production batches.
• Collaborate with cross‑functional teams to optimize process efficiency and reduce costs.
• Develop and implement strategies to enhance product quality and yield.
• Monitor and control processes to prevent contamination or defects.
• Experience in microbial processing, downstream processing, mammalian cell culture, and upstream processing.
• Strong understanding of downstream processing techniques including filtration, centrifugation, and chromatography.
• Experience working in a regulated environment (cGMP).
• Ability to work collaboratively with cross‑functional teams.
• Strong problem‑solving skills and attention to detail.
• Familiarity with quality control measures and regulatory requirements.