API Manufacturing Technician

Eurofins USA PSS Insourcing Solutions; Groton (CT); On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

Comprehensive medical coverage

401(k) with company match

Paid vacation and holidays

Job summary

A leading pharmaceutical manufacturing firm is seeking a dedicated individual to join their team in Groton, CT. This full-time position involves responsibilities in cGMP production processes including executing detailed procedures and managing equipment. The ideal candidate will have a high school diploma with 4+ years of experience in a cGMP environment. Strong troubleshooting skills, attention to detail, and effective communication are essential. The role offers excellent benefits and requires the ability to work overtime as needed.

Qualifications

• 4+ years of relevant experience in a cGMP manufacturing environment.
• Ability to work independently as part of a matrix development team.
• Physical capability to lift over 50 lbs and stand for extended periods.

Responsibilities

• Execute Process Operating Instructions in a cGMP environment.
• Conduct equipment preparation, adjustment, monitoring, and cleaning.
• Identify and report process deviations impacting product quality.

Skills

cGMP environment experience

Troubleshooting and problem-solving skills

Workload planning and organization

Written and verbal communication

Microsoft Office proficiency

Education

High School Diploma or GED

Associate degree (Science or technical discipline)

Tools

Delta V Production Control System

Job description

Job Description

You will be part of a multi-disciplinary team responsible for the Current Good Manufacturing Practices (cGMP) production of non-commercial size clinical batches supporting Active Pharmaceutical Ingredient (API) development. This includes but is not limited to: supporting the manufacturing operations team, reviewing Standard Operating Procedures, executing batch records, and supporting commissioning and qualification of process equipment. Standard work will involve chemical synthesis of API, which includes these operational tasks: solid / liquid charges to vessels, atmospheric / vacuum distillations, liquid‑liquid extractions, phase cut, crystallization, filtrations and drying.

ROLE RESPONSIBILITIES

• Execute Process Operating Instructions in a cGMP {part of GxP} environment.
• Responsible for equipment preparation, operational adjustment, process monitoring, sampling, and equipment cleaning of complex pharmaceutical manufacturing equipment as defined in standard operating procedures.
• Perform manual handling tasks, including lifting, carrying and moving objects weighing up to and exceeding 50 pounds on a routine basis throughout the work shift, using proper material‑handling techniques and safety practices.
• Handle and segregate manufacturing waste in accordance with approved waste management, environmental, and safety requirements.
• Support equipment qualification/ commissioning activities.
• Adhere to cGMP and standard and local operating procedure requirements.
• Complete recurring assignments independently and select the most appropriate method or approach to do so within prescribed limits of authority.
• Identify opportunities for continuous improvements and enable implementation.
• Maintain cross‑functional communication with tech transfer team: Compliance, Quality, Process Chemists, Analysists, and Process Supervisors.
• Perform troubleshooting of manufacturing support equipment and operations.
• Generate, assist, and execute documentation associated with cGMP API manufacture, such as working batch record and cleaning documentation and in‑process control sampling.
• Support Standard Operating Procedure Periodic Reviews.
• Report any deviations or observations that might lead to adverse impact on product quality or process safety.
• Actively participate in shift exchange activities and communication channels.
• Complete training to take part in safety inspections within the facility.
• Manage own time, professional development, and be accountable for own results.
• Prioritize own workflow and assist in prioritizing the workflow of less‑experienced colleagues.

Qualifications

BASIC MINIMUM QUALIFICATIONS

• High School Diploma or GED
• 4+ years of relative experience
• Demonstrated experience in a cGMP manufacturing environment.
• Operational knowledge of Production Control Systems
• Ability to think critically and demonstrate troubleshooting and problem‑solving skills
• Strong workload planning skills, organization, attention to detail, and follow through
• Demonstrated capability to work as an independent contributor within a matrix development team
• Candidate must be physically capable of standing for prolonged periods, able to lift up to or in excess of 50 lbs, be amenable to wearing personal protective equipment and working with hazardous materials.
• Excellent written and verbal communication skills
• Strong computer skills in Microsoft Office required e.g. MS Word, MS Excel

PREFERRED QUALIFICATIONS

• Associate degree (Science or technical discipline)
• Strong mechanical aptitude and desire to execute hands on manual labor
• Experience with Delta V Production Control System
• Experience in a Pharmaceutical cGMP manufacturing environment
• Experience performing large scale distillations / Filtrations / milling

Additional Information

• The position is full‑time, Monday through Friday, 8 a.m. to 5 p.m.,
• May be requested to work on weekends, overtime, and holidays based on business needs.
• Candidates currently living within a commutable distance of Groton, CT are encouraged to apply.
• Ability to work overtime as required.
• Excellent full‑time benefits, including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
• #LI-EB1
• Authorization to work in the United States indefinitely without restriction or sponsorship

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.