Pharma Process Technician — Shift (GMP)

Croda Singapore

Alabaster (AL)

On-site

USD 52,000 - 76,000

Full time

14 days+
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Benefits offered by this job

Excellent Medical, Dental, and Vision
Wellness Reimbursement
Career Development
Company paid Life and AD&D Insurance
Short- and long-term disability

Job summary

Croda is seeking a Shift Process Technician in Alabaster, AL to safely perform production duties, operate vessels, and carry out bulk organic synthesis and purification of pharmaceutical products. All work follows Safety, Health and Environmental guidelines, government regulations, cGMP manufacturing, and established procedures.

Required: BS in chemistry/chemical engineering or related field, 1 year pharma manufacturing experience in a cGMP environment, strong attention to detail, integrity, and

Qualifications

  • Bachelor degree in chemistry, chemical engineering, biology, or related field preferred.
  • 1 year experience in pharmaceutical manufacturing in a cGMP environment preferred.
  • High level of integrity and reliability.
  • Excellent written and verbal communication skills.

Responsibilities

  • Understand and follow procedures to operate safely and in compliance with cGMP, OSHA, and safety guidelines.
  • Perform synthesis and purification of pharmaceutical products and document work.
  • Access electronic procedures and Master Control regularly.
  • Assist in troubleshooting, calibrating, and preventive maintenance of equipment.
  • Maintain knowledge of cGMP and manufacturing compliance.
  • Execute manufacturing SOPs/BPRs accurately and timely.
  • Perform facility sanitation and maintenance; sanitize glassware and equipment.

Skills

Attention to detail
Integrity
Strong communication
MS Office proficiency
Teamwork / independent work

Education

Bachelor of Science in chemistry or chemical engineering or related field

Job description

Croda is seeking a Shift Process Technician in Alabaster, AL to safely perform production duties, operate vessels, and carry out bulk organic synthesis and purification of pharmaceutical products. All work follows Safety, Health and Environmental guidelines, government regulations, cGMP manufacturing, and established procedures.

Required: BS in chemistry/chemical engineering or related field, 1 year pharma manufacturing experience in a cGMP environment, strong attention to detail, integrity, and

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