Pharma Shift Process Technician – cGMP

Croda

Alabaster (AL)

On-site

USD 55,000 - 75,000

Full time

12 days ago
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Benefits offered by this job

Medical coverage
PTO
401K match
Wellness reimbursement
Parental leave
Career development
Life/AD&D insurance
Disability coverage
Paid holidays

Job summary

Croda in Alabaster, AL, is seeking a Shift Process Technician to safely manage the operational side of production, including charging of raw materials, vessel operations, and bulk organic synthesis with purification of pharmaceutical products.

The role requires a BS in chemistry/engineering or related field, 1 year pharma manufacturing experience in a cGMP environment, strong attention to detail, integrity, and the ability to follow SOPs and QMS while collaborating with QC, R&D, QA and

Qualifications

  • Bachelor of Science in chemistry, chemical engineering, biology, or related field preferred.
  • 1 year experience in pharmaceutical manufacturing in a preferred cGMP environment.
  • Strong attention to detail.
  • High level of integrity and reliability.
  • Working knowledge of Quality Management System in laboratory environment.
  • Intermediate math skills.
  • Intermediate mechanical skills required for manipulation of manufacturing equipment, such as glassware, glass reactors, pressure reactors, balances, Nutsche pressure filters, and gas cylinders.
  • Excellent written and verbal communication skills.
  • Self-motivated.
  • Proficient in basic applications such as Word, Excel, Outlook.
  • Ability to manage and complete multiple tasks simultaneously.
  • Ability to work both in a team environment and work independently.

Responsibilities

  • Understand and follow established procedures to operate safely, in an environmentally sound manner, and according to cGMP including during emergencies, startup & shutdown, and OSHA related issues.
  • Perform synthesis and purification of pharmaceutical products and fully document work.
  • Access electronic communication and procedures regularly (e.g., email, Master Control).
  • Assist in troubleshooting, calibrating, and performing preventative maintenance on manufacturing equipment.
  • Knowledge of personal protective equipment and use.
  • Hold others accountable for safety and elevate issues as necessary.
  • Perform inventory control of reagents and supplies.
  • Complete drum movement training, and perform physical labor associated with movement.
  • Maintain an elementary understanding of cGMP and compliance in a manufacturing setting.
  • Accurately and timely execute manufacturing SOPs/BPRs.
  • Perform facility sanitation and maintenance.
  • Sanitation of glassware, equipment, and fume hoods.
  • Replace compressed gas cylinders.
  • Complete respirator fitting and training.
  • Perform label printing and verification.
  • Perform upkeep of employee training records.
  • Report and address any problems in daily manufacturing.
  • Conduct laboratory duties in a cGMP/QMS environment.
  • Perform as SME for QC/QA investigations.
  • Transfer hazardous or nonhazardous waste materials to collection areas for disposal or recycling.
  • Prepare and align individual performance goals with department goals.
  • Complete company-required training programs.
  • Adhere to all applicable regulations, policies, and procedures for health, safety, and environmental compliance as outlined in the company\'s Standard Operating Procedures, Chemical Hygiene Plan, Emergency Contingency Plan, training memoranda, policy memoranda, Safety Data Sheets, Specification Records, etc.
  • The job function routinely works with chemicals, organic solvents, and biological samples, and may on occasion require work with caustic chemicals.
  • Requires the ability to gown and wear safety attire as well as any required protective equipment including safety glasses.
  • Meeting hygiene and health requirements to comply with a cGMP environment.
  • Effectively communicate with cross-functional teams including QC, R&D, QA, and Management
  • Occasionally lift and/or moving items up to 50 pounds and manipulating drums (max. weight ∼ 650 pounds) using an appropriate drum handler.

Skills

Attention to detail
Integrity and reliability
QMS knowledge
Math skills
Mechanical skills
Communication skills
Word Excel Outlook
Team player

Education

Bachelor of Science in chemistry or related field

Job description

Croda in Alabaster, AL, is seeking a Shift Process Technician to safely manage the operational side of production, including charging of raw materials, vessel operations, and bulk organic synthesis with purification of pharmaceutical products.

The role requires a BS in chemistry/engineering or related field, 1 year pharma manufacturing experience in a cGMP environment, strong attention to detail, integrity, and the ability to follow SOPs and QMS while collaborating with QC, R&D, QA and

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