Referso Jobs

Manufacturing Biotech Associate

MSD · Posted Oct 30, 2026

Open

Dunboyne, Meath, Ireland
On-site
Associate
Visa sponsorship

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Manufacturing Biotech Associate

MSD · Posted Oct 30, 2026

Open

Dunboyne, Meath, Ireland
On-site
Associate
Visa sponsorship

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Quality Data Associate Specialist

MSD · Posted Oct 28, 2026

Open

Haarlem, North Holland, Netherlands
On-site
Temporary · Associate
1+ years

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De Quality Data Associate Specialist speelt een sleutelrol in het beheren en borgen van kwaliteitsdata en -processen binnen het Quality Release-team in Haarlem.

Compensation

Een competitief salaris, 35,5 vakantiedagen, 8% vakantietoeslag en 3% eindejaarsuitkering, Incentive Plan, Een uitzekend pensioen

Responsibilities

Onderunt afdelingen bij het implementeren van wijzigingen in richtlijnen via o.a. Veeva, Veeva Registrations en Change Control-processen
Dagt actief bij aan het vergroten van het kwaliteitsbewustzijn binnen de organisatie en fungeert als vertegenwoordiger van Quality binnen verschillende systemen
Neemt deel aan introducties van nieuwe producten, waarbij je verantwoordelijk bent voor de kwaliteitsaspecten
Bent Quality Assurance-verantwoordelijk voor een aantal producten
Controleert en keurt masterdata (ZERT, ZERP en ZDSB) goed

Requirements

Bachelor or Masterdiploma in farmacie
life sciences
procestechnologie
chemie
Nice to have: SAP

Skills

Analytical Problem Solving Aseptic Filling cGMP Compliance Complaint Management

Químico Analista de Soporte Analítico (Posicion Temporal - 12 meses)

Pfizer · Posted Nov 6, 2026

Open

Toluca, Mexico
On-site
Contract
4+ years

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Support the planning and execution of analytical method validation activities for chemical and physicochemical methods in a GMP-regulated laboratory.

Responsibilities

Support planning and execution of analytical method validation activities
Prepare and organize samples, standards, reagents, solutions, reference materials and documentation
Execute validation tests such as specificity, accuracy, precision, linearity, range, robustness, system suitability, detection limit, quantitation limit and method equivalency
Ensure training records reflect current qualification
Verify instrument readiness, calibration status and system suitability

Requirements

Bachelor's degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, Biology, Biochemistry or related scientific discipline
Nice to have: HPLC
Nice to have: GC
Nice to have: UV-Vis
Nice to have: dissolution

Skills

analytical method validation verification transfer lifecycle activities GMP

Químico Analista de Soporte Analítico (Posicion Temporal - 12 meses)

Pfizer · Posted Nov 6, 2026

Open

Toluca, Estado de México, Mexico
On-site
Temporary · Associate
4+ years

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Support the planning and execution of analytical method validation activities for chemical and physicochemical methods in accordance with approved protocols.

Responsibilities

Support the planning and execution of analytical method validation activities for chemical and physicochemical methods in accordance with approved protocols.
Prepare and organize samples, standards, reagents, solutions, reference materials, and documentation required for validation studies.
Execute validation tests such as specificity, accuracy, precision, linearity, range, robustness, system suitability, detection limit, quantitation limit, and method equivalency, as applicable.
Ensure training records reflect current qualification to perform validation, verification, and routine analytical method activities.
Verify instrument readiness, calibration status, analytical conditions, and system suitability requirements before executing validation or verification testing.

Requirements

Bachelor's degree in Chemistry
Pharmaceutical Sciences
Chemical Engineering
Biology
Biochemistry

Skills

Analytical method validation Good Manufacturing Practices (GMP)

Manager, Quality Assurance Second Shift

MSD (I.A.) LLC, TW Branch · Posted Nov 4, 2026

Open

Durham, North Carolina, United States
On-site
Full-time · Manager
$96K–$151K per year
5+ years

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Lead and manage Shop Floor Quality Assurance team on second shift, ensuring compliance with cGMP and company quality systems.

Compensation

$96,200.00 - $151,400.00

Responsibilities

Lead a Shop Floor QA team to provide end-to-end QA support for Production Support & Media, Drug Substance and Drug Product throughout the project lifecycle.
Ensure all aspects of the Shop Floor QA proceed in compliance with cGMP, regulations, and our Company’s Quality Management System focusing on batch record review, process/aseptic observations, critical site review, critical alarm management, environmental monitoring incursion/excursion response.
Support Operations and the Technical Operations Deviation Management groups with event assignments, classifications, investigations, corrective and preventative actions, reviews and approvals through current Quality Systems (e.g., CLUE and SAP).
Support and maintain a "Safety First", " Quality Always" environment with participation in Site GEMBAs for Safety and Quality Compliance.
Escalate and collaborate quality and compliance issues as needed through established site Tiers.

Requirements

Bachelor’s degree in chemical engineering, biochemical engineering, biological systems engineering, biology, biochemistry, chemistry or related life science or engineering discipline
Master’s degree in chemical engineering, biochemical engineering, biological systems engineering, biology, biochemistry, chemistry or related life science or engineering discipline

Laboratory Technician

Novo Nordisk A/S · Posted Nov 6, 2026

Open

Bagsværd, Capital Region of Denmark, Denmark +1 more
Contract
DKK 438K–DKK 643K per year

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Laboratory Technician in QC Stability 2 in Bagsværd, responsible for handling samples, establishing stability studies, and supporting stability activities.

Locations (2)

Bagsværd, Capital Region of Denmark, Denmark
Hillerød, Capital Region, Denmark

Compensation

The Annual Base Salary ranges from 437,600.00 to 643,200.00 DKK, corresponding to the level of the position.

Responsibilities

Handling samples, including packing, withdrawing samples from stability chambers and sending them for analysis
Establishing stability studies in gLIMS (Global Laboratory Information Management System)
Handling simulations, including in-use studies, temperature cycling studies and light studies
Coordinating sample logistics with relevant stakeholders
Reviewing study protocols

Requirements

Laboratory Technician (Laborant), Bioanalytiker or equivalent
Nice to have: experience with stability studies

Manufacturing Biotech Associate

Manufacturing Biotech Associate

Responsibilities

Requirements

Skills

Quality Data Associate Specialist

Compensation

Responsibilities

Requirements

Skills

Químico Analista de Soporte Analítico (Posicion Temporal - 12 meses)

Responsibilities

Requirements

Skills

Químico Analista de Soporte Analítico (Posicion Temporal - 12 meses)

Responsibilities

Requirements

Skills

Manager, Quality Assurance Second Shift

Compensation

Responsibilities

Requirements

Laboratory Technician

Locations (2)

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Benefits

Skills

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GLIMS jobs

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Requirements

Skills

Compensation

Responsibilities

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Skills

Responsibilities

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Skills

Compensation

Responsibilities

Requirements

Locations (2)

Compensation

Responsibilities

Requirements

Benefits

Skills

Benefits

Skills

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