Referso Jobs

Analyst 3 - Quality Assurance

Artech LLC · Posted Nov 9, 2026

Open

Wilson, North Carolina, United States
On-site
Full-time · Associate
$60–$62 per hour
2+ years

Analyst 3 - Quality Assurance

Artech LLC · Posted Nov 9, 2026

Open

Wilson, North Carolina, United States
On-site
Full-time · Associate
$60–$62 per hour
2+ years

Manufacturing Technician II (Crosslink), 2nd Shift 10am-6:30pm

Anika Therapeutics · Posted Nov 9, 2026

Open

Bedford, Massachusetts, United States
2–4 years

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Responsible for cross-linked hyaluronic acid product production, operating equipment, cleaning, troubleshooting, and documentation in a cGMP environment.

Compensation

The salary range provided is based on the Company’s reasonable estimate of the base salary pay range for this position at the time of posting. Actual base pay is determined by several factors relevant to the position, including skills, competencies, experience, education, and geographic location. Anika also offers a discretionary bonus program for all full-time employees, comprehensive healthcare benefits, health savings account, 401(k) plan with up to 5% company match which includes immediate vesting, employee stock purchase plan at a 15% discount, accrued paid time off, additional long-term incentives including stock awards, and much more.

Responsibilities

Operates production equipment according to SOPs, Batch Records, MD, and OPM.
Executes all procedures associated with cross-linked hyaluronic acid product production.
Adheres strictly to written work instructions to perform solvent recovery, COP, and CIP of complex equipment and components.
Performs scheduled cleaning and sterilization of equipment.
Supports changeover activities.

Requirements

High school diploma or GED, or equivalent experience.
Nice to have: Manufacturing experience in the medical device industry
Nice to have: Experience working in a clean room or using aseptic technique
Nice to have: Experience using commercial-scale automated equipment

Skills

cGMP experience

Automation Engineer - DeltaV

FUJIFILM Middle East & Africa · Posted Jun 11, 2026

Open

Billingham, England, United Kingdom
7+ years

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Automation Engineer with deep Emerson DeltaV expertise to support, enhance, and expand site Automation systems in a cGMP environment.

Compensation

Competitive salary, with 35 days holiday (Not including Public Holidays), annual incentive plan and up earn up to 21% on your pension

Responsibilities

Deploy, maintain, and optimize site Automation systems with a focus on DeltaV
Provide front-line support to Process Owners: diagnose, troubleshoot, and resolve automation issues
Deliver small projects and CI initiatives, including change controls and validation/qualification deliverables
Prepare and review technical proposals, scope and cost estimates, and resource plans for process control work
Create/update lifecycle documentation: SOPs, periodic reviews, maintenance plans; sustain validated status for GMP systems

Requirements

HND or equivalent (e.g., time-served apprenticeship) in EC&I

Skills

DeltaV software design DeltaV development hardware integration DeltaV Batch configuration

Specialist QA Shop Floor

Bristol Myers Squibb · Posted Nov 5, 2026

Open

Summit, New Jersey, United States
On-site
Full-time · Associate
$35–$42 per hour
2+ years

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The Quality Assurance Shop Floor team provides 24x7 Quality collaboration and oversight of site operations, including Manufacturing, Quality Control, Label Operations and Warehouse Operations ensuring compliance with cGMP.

Compensation

$34.92 - $42.32 hour

Responsibilities

Provide routine Quality-the-floor oversight and triage unexpected events
Identify departures from approved procedures and respond to issues
Document operational verification within Manufacturing Execution System (MES)
Review manufacturing records to ensure compliance with approved procedures
Maintain compliance with assigned learning plan

Requirements

Bachelor's degree in STEM field
High school diploma
Associate’s degree with equivalent combination of education and experience
Nice to have: FDA/EMA regulations
Nice to have: biopharmaceuticals

Skills

cGMP experience batch record review change control product complaints deviations

Sr. Process Engineer

PCI Pharma Services · Posted Nov 6, 2026

Open

San Diego, California, United States
On-site
Full-time · Senior
$107K–$134K per year
8+ years

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Design and optimize pharmaceutical and biopharmaceutical manufacturing processes for improved efficiency and yield. Supports manufacturing operations and mentor junior engineers. Lead technical assessment and improvement/scale up projects for manufacturing processes, including managing projects through to successful completion.

Compensation

The base salary hiring range for this position is $106,800 - $133,500 plus eligibility for an annual performance bonus.

Responsibilities

Design and specify processes and manufacturing equipment systems
Evaluate existing systems for continuous improvement
Provide in-depth technical review of all documents
Research new technologies and implement new/upgraded systems
Document changes to systems per change management procedures

Requirements

Bachelor's degree
Bioengineering
Chemical Engineering
Electrical Engineering
Industrial Engineering

Skills

cGMP experience manufacturing processes process flow troubleshooting GMP regulations

Associate II, Shop Floor Quality Assurance Cell Therapy

Bristol Myers Squibb · Posted Nov 5, 2026

Open

Devens, Massachusetts, United States
On-site
Full-time · Entry
$35–$43 per hour
0–2 years

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The Quality Assurance Shop Floor team is responsible for 24x7 Quality collaboration and oversight of site operations, including but not limited to Manufacturing, Quality Control laboratories, and Supply Chain Operations.

Compensation

The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities.

Responsibilities

Provide Quality on-the-floor oversight to Manufacturing/ QC/ Supply Chain Operations & responding to minor issues or escalating to senior members.
Perform and document operational verification per approved procedures.
Observe manufacturing operations and identify departures from clean room behaviors and aseptic techniques.
Provide quality oversight to maintenance operations and support pre-approved return to service plans.
Perform area walkthroughs to identify quality issues and support remediation to ensure the floor and operations are in adherence with cGMP and approved procedures.

Requirements

Bachelor's degree in STEM field preferred
High school diploma/ Associates degree with equivalent combination of education and work experience may be considered
Nice to have: biopharmaceuticals manufacturing
Nice to have: cell therapy manufacturing

Skills

cGMP experience

GMP Warehouse Specialist

Evotec · Posted Nov 5, 2026

Open

Abingdon, Oxfordshire, United Kingdom
On-site
Full-time · Mid
£35K per year

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Experienced Warehouse Specialist working within a GMP Warehouse to manage materials, receipts, forklift operations, and general warehouse duties.

Compensation

£35,000, plus excellent benefits package

Responsibilities

Ensure all activities are conducted in a safe manner and that all equipment and racking is regularly checked and complies with Safety Legislation
The effective and efficient receipt of goods through a centralised receipting location
Managing GMP materials (raw materials and consumables) through receipt, sampling and location transfer
Loading and unloading vehicles (manually and using FLT)
General warehouse duties

Requirements

Nice to have: SAP

Skills

Warehouse ERP Systems Forklift truck experience cGMP Experience COSHH regulation Microsoft Excel SAP

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