Referso Jobs

CQV Engineer II

PM Group · Posted Nov 9, 2026

Open

Conshohocken, Pennsylvania, United States
3–5 years

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CQV Engineer II

PM Group · Posted Nov 9, 2026

Open

Conshohocken, Pennsylvania, United States
3–5 years

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CQV Engineer III

PM Group · Posted Nov 9, 2026

Open

Conshohocken, Pennsylvania, United States
Hybrid
Full-time · Mid
5–10 years

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The CQV Engineer III position is an exciting opportunity to join PM Group’s quickly growing Outsourced Technical Services(OTS) team. This role requires an understanding of the technical aspects of commissioning (Cx), qualification and validation (CQV), as well as an understanding and applying the principals of good documentation practices (CGDP).

Responsibilities

Performs work in compliance with PM Group’s Service Delivery Platforms and Quality Management System (QMS)
Independently interact with client to assess and continuously reassess client needs
Perform quality GAP analysis
Author technical and scientific reports
Demonstrates an understanding of project scope of work assigned

Requirements

Bachelor’s degree
Engineering degree (preferred)
Nice to have: Pharmaceutical industry
Nice to have: Life Sciences
Nice to have: Biotech

Skills

CQV Commissioning (Cx)Qualification Validation CGDP cGMP FAT

Consultant - Business Consulting Risk - TMT - CNS - RISK - DIGITAL RISK

EY · Posted Nov 7, 2026

Open

Mumbai, Maharashtra, India
On-site
Full-time · Mid
2–13 years

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Consultant role within TMT Business Consulting Risk, focusing on Digital Risk and Computer System Validation (CSV) for Life Sciences clients.

Responsibilities

Perform assessments of computer systems and processes for Life Sciences clients
Create/ review CSV deliverables like user requirements, system specifications, Validation Plan, Qualification Plans, SOPs, IQ/OQ/PQ, Traceability matrix, Design Specs, and validation summary reports
Provide guidance and oversight of validation activities for projects involving GxP relevant computer systems
Work closely with project team members to incorporate appropriate elements of quality and compliance into the system lifecycle
Review and approve computer system validation work products, assuring thoroughness of validation planning and making appropriate progress towards timely completion of validation deliverables

Requirements

Bachelor of Technology in Computer Science
B pharmacy
Bachelor of Computer Applications
Nice to have: HPALM
Nice to have: Azure DevOps (ADO)

Skills

Computer System Validation Quality and Compliance Enterprise Applications

Manufacturing Specialist 1 - Reagents

Singular Genomics · Posted Nov 5, 2026

Open

San Diego, California, United States +1 more
0–2 years

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Responsible for executing work orders, preparing reagent buffers, and maintaining manufacturing records and equipment in a regulated laboratory environment.

Locations (2)

San Diego, California, United States
California, United States

Compensation

This role is eligible for to receive equity as part of the compensation package.

Responsibilities

Familiar with 5S and other lean six sigma principles
Identify process inefficiencies and suggest improvements
Prepare reagent buffers upwards of 200 L in accordance with SOPs, PBRS, and current good documentation practices (cGDP)
Use balances, scales, mixers, pH meters, conductivity meter, refractometers, and other laboratory equipment
Package, label, fill/seal reagents using automated and manual fill systems

Requirements

Bachelor of Science degree in a scientific field preferred

US_MFG Associate, Filling and Visual Inspection

Boehringer Ingelheim · Posted Nov 5, 2026

Open

Fremont, California, United States
Associate
$54K–$80K per year
1+ years

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The Manufacturing Associate, Filling and Visual Inspection executes routine unit operations in Filling or Visual Inspection manufacturing as assigned related to the manufacturing of drug product in a multi-product facility.

Compensation

The base salary range for this position is $53,600 to $80,400. The position may be eligible for a role-specific discretionary bonus, relocation assistance, and/or other compensation elements.

Responsibilities

Under routine supervision, performs basic Filling or Visual Inspection operations and advanced operations.
Supports continuous improvement projects of low to moderate complexity in the production areas.
Responsible for basic interactions such as shift change pass down and coordination between other departments.
Performs internal support duties including stocking consumables/materials, appropriately discarding expired reagents, recognizing, and reporting process and equipment anomalies.
Maintains production areas according to predefined standards (5s).

Requirements

High School degree plus minimum one (1) year work experience in GMP regulated industry; Associate/Bachelor degree from an accredited institution or biotechnology vocational training preferred.
Nice to have: Associate/Bachelor degree
Nice to have: biotechnology vocational training

Skills

cGMP regulated industry

QC Analyst II

Lonza · Posted Nov 4, 2026

Open

Pearland, Texas, United States
On-site
Full-time · Associate

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The purpose of this role is to perform Quality Control assays for product release of cell therapy products, Raw Material Release and Stability Studies.

Compensation

Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.

Responsibilities

Perform Quality Control assays for product release of cell therapy products, Raw Material Release and Stability Studies
Maintain data and follow cGMP regulations including writing deviations and other Quality documentation
Use extensive knowledge of defined SOPs & policies to make sound decisions
Record test results and maintain raw data accurately
Effectively present information and ideas, facilitating understanding among team members

Requirements

Bachelor's degree in a relevant science field

Skills

biological, cell-based assays flow cytometry cGMP cGDP spreadsheets databases

QC Analyst II (PM Shift)

Lonza · Posted Nov 4, 2026

Open

Pearland, Texas, United States
On-site
Full-time · Associate

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Perform Quality Control assays for product release of cell therapy products, Raw Material Release and Stability Studies while following cGMP regulations.

Compensation

This is a competitive, hourly paid position.

Responsibilities

Perform Quality Control assays for product release of cell therapy products, Raw Material Release and Stability Studies.
Maintain data and follow cGMP regulations including writing deviations and other Quality documentation.
Use extensive knowledge of defined SOPs & policies to make sound decisions.
Record test results and maintain raw data accurately.
Effectively present information and ideas, facilitating understanding among team members.

Requirements

Bachelor's degree in a relevant science field

Skills

biological, cell-based assays flow cytometry cGMP cGDP lab equipment operation spreadsheets

E&I Technician

Accord Healthcare · Posted Nov 5, 2026

Open

Fawdon, Newcastle upon Tyne, United Kingdom
On-site
Full-time · Mid

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To ensure the continued operation of the calibration systems and equipment within the company, focusing on instrumentation and calibration alongside general electrical duties.

Compensation

Competitive + bonus + benefits

Responsibilities

Troubleshoot, repair, maintain, calibrate, alter / modify equipment and systems to the company calibration and regulatory standards and electrical equipment and systems to current regulations.
Troubleshoot, maintain, adjust, and repair, calibrate, and install equipment with calibration functions, controllers, electronic circuits, and mechanical components.
Use test equipment and instruments to calibrate, repair and test apparatus, equipment and systems.
Working from drawings, layouts and other specifications to fault find and diagnose problems in the systems or equipment.
Competent in the sites BMS/EMS systems.

Requirements

ONC level or equivalent in an Electrical Engineering or Instrumentation discipline
Nice to have: Compex 5&6
Nice to have: 18th edition

Skills

analogue/digital signals communication protocols 0-10V

Senior Analyst, Quality Control

Endo · Posted Jan 12, 2026

Open

Pudupakkam, Tamil Nadu, India
On-site
Senior

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To perform analysis of in-process samples, hold time, finished product samples, WRS qualification, instrument calibration, and other analytical testing based on routine requirements.

Responsibilities

Perform analysis of In-process sample, Hold Time, Finished product samples, WRS Qualification, Instrument Calibration and any other analytical testing
Report and document analytical data as per good laboratory practices and Good documentation practices
Perform analytical method transfer, method verification/validation
Maintain working area, documents, and records in an auditable manner
Follow safety, cGLP, and cGDP in work area

Skills

Good laboratory practices Good documentation practices cGLP cGDP Analytical method transfer Method verification/validation Instrument Calibration

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