QC Associate Job at Proclinical (Visp)

Quality Control Associate I, Reagents

The Quality Control Associate I, Reagents will be responsible for executing core...

Location

United States , Austin, Texas

Salary:

Not provided

Diasorin

Expiration Date

Until further notice

Requirements

Bachelor's Degree B.S. in Chemistry, Biochemistry, Biology, or related science discipline required
At least 1 year of relevant experience in a Life Sciences, Chemistry, or Medical Technology related industry preferably in an FDA regulated and/or ISO certified operation required

Job Responsibility

Deliver timely and accurate Quality Control testing for bioassay and core consumable products
Deliver timely and accurate completion of quality control and manufacturing process documentation including related business system transactions
Generate Certificates of Quality
Document and complete non-conformances
Respond appropriately to environmental monitoring notifications of specialized storage areas
includes 24/7 call list rotation
Execute stability study sample scheduling and processing
Participate in program to sustain orderliness and cleanliness within related quality control and manufacturing area
Assist in timely processing of purchased materials for release including related business system transactions
Assist in on-time maintenance and calibration of Reagent QC measuring and monitoring devices

What we offer

Receive a competitive salary and benefits package as you grow your career at DiaSorin

Fulltime

Quality Control Inspector II

The Quality Control Inspector II (MRB) will be responsible for executing Quality...

Location

United States , Austin, Texas

Salary:

Not provided

Diasorin

Expiration Date

Until further notice

Requirements

H.S. Diploma or equivalent required
Associate's Degree in a technical field preferred
5+ Years relevant work experience or training required
7+ Years related experience without Associate's degree
Zeiss CMM experience preferred

Job Responsibility

Lead or assist the Material Review Board process
Process purchased materials for release
Application of GD&T practices
Take ownership and assist in core QC functions and associated activities relating to Incoming Product Control
Fulfill individual and departmental CAPP objectives
Assist and document the investigation and resolution of problems initiated through non-conformances, corrective action, customer complaints, and/or audit findings
Coordinate and/or conduct departmental maintenance and calibration of local measuring and monitoring devices
Schedule outsourced testing and services
Maintain cleanliness and integrity of facilities and working areas
Lead and assist with departmental document change control and engineering change control activities, monitor and assess impact of procedural and engineering change releases

What we offer

Receive a competitive salary and benefits package as you grow your career at Diasorin

Fulltime

QC Associate (Raw Materials)

ABOUT THE JOB Conduct testing of raw materials, especially water samples, in lin...

Location

Singapore

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

Requirements

Experience in a GMP-regulated QC environment
Hands-on experience with water testing (TOC and Conductivity) and laboratory instrumentation
Degree in Chemistry, Biochemistry, or a related scientific discipline
Demonstrates a methodical approach, strong attention to detail, and the ability to work independently

Job Responsibility

Conduct testing of raw materials, especially water samples, in line with current good manufacturing practices (GMP)
Perform analytical tests including Total Organic Carbon (TOC) and Conductivity measurements
Operate and maintain relevant laboratory equipment
Ensure proper documentation of all results and support data integrity practices
Collaborate with quality, production, and laboratory teams to uphold compliance and resolve potential deviations
Participate in internal audits and contribute to the continuous improvement of laboratory processes

What we offer

Global Diversity: Be part of an international team of 110+ nationalities
Trust and Growth: 70% of our leaders starting at entry-level
Continuous Learning: Internal Academy and over 250 training modules
Vibrant Culture: Afterworks, networking events
Meaningful Impact: CSR initiatives, including the WeCare Together program

Fulltime

Sr. QC Associate I

10x Genomics is looking for a Sr. QC Associate I to join our Quality Control tea...

Location

United States , Pleasanton

Salary:

37.64 - 50.91 USD / Hour

10x Genomics

Expiration Date

Until further notice

Requirements

B.S. in Analytical Chemistry, Biochemistry, or a related field
5+ years of laboratory experience specifically in a QC environment
Strong hands-on experience with NGS and tissue-based assays (including immunofluorescence and flow cytometry)
Proficiency in PCR, qPCR, spectrophotometry, spectrofluorometry, and HPLC
Experience collaborating with R&D and QA on risk-based QC strategy assessment including assay robustness, assay cost, and alignment of QC checkpoints to the manufacturing process
A solid understanding of New Product Introduction (NPI) and manufacturing processes
Ability to manage and track diversified QC assays and projects in a rapidly evolving environment
Strong critical thinking, logical problem-solving skills, and the ability to communicate effectively with stakeholders

Job Responsibility

Execute QC Testing: Perform quality control operations according to defined procedures to ensure the integrity and quality of raw materials, intermediates, and finished goods
Data Analysis & Disposition: Complete QC testing in a timely manner and disposition materials based on established acceptance criteria
Product Development and Sustaining Support: Serve as the primary QC point of contact to oversee project completion, providing expert guidance on assay setup and assisting in the introduction and optimization of new products and processes
Assay Cross-Training: Cross-train on various inspections, including first article inspection, metrology, microscopy, analytical assays, and NGS
Documentation: Maintain quality control batch records and ensure Good Documentation Practices (GDP) under ISO requirements. Accurately track QC test data, calibration records, and inventory. Draft Work Instructions in collaboration with the Manufacturing Systems & Engineering team
Quality Compliance: Initiate non-conformance, deviation reports, engineering change orders (ECO) and follow up on necessary action items. Ensure that lab operations and workflow execution are compliant with ISO requirements
Problem Solving: Effectively identify and communicate complications arising from QC testing with minimal supervision. Work closely with scientists to establish and maintain technical solutions. Drive completion of investigations and minimize disruptions to QC operations

What we offer

Equity grants
Comprehensive health and retirement benefit programs
Annual bonus program or sales incentive program
Generous time off
Competitive and comprehensive health benefits package
Family friendly policies like parental leave

Fulltime

QC Associate II

As a QC Associate II, you will be responsible for inspecting raw materials, inte...

Location

United States , Pleasanton

Salary:

31.78 - 43.03 USD / Hour

10x Genomics

Expiration Date

Until further notice

Requirements

B.S. in Biological Engineering, Molecular Biology, Analytical Chemistry, Chemical Engineering, or related discipline
3 years of relevant laboratory experience in manufacturing and QC of life science products (e.g., PCR, NGS, protein analysis, HPLC)
Willingness to rotate through various laboratory and administrative tasks and ability to prioritize workload, and adhere to deadlines
Proficiency in data entry using tools such as Excel, Oracle ERP and LIMS
Demonstrated ability to work both independently and as part of a team
Strong attention to detail, organization, and commitment to quality
Effective communication and observational skills
Excellent critical and logical thinking skills to analyze and troubleshoot issues

Job Responsibility

Conduct quality control testing on raw materials, intermediates, and finished products according to established procedures
Perform molecular biology techniques, including PCR, next-generation sequencing, microscopy, cell and tissue based assays, and HPLC
Participate in instrument QC workflows, including training to work with mechanical stages and read technical drawings and first article inspection report
Accurately follow work instructions and standard operating procedures, while proactively identifying and reporting discrepancies
Maintain comprehensive and accurate records, including QC batch files and Receiving Inspection Reports, in accordance with Good Documentation Practices
Efficiently communicate complications identified during QC testing and collaborate with engineers and scientists to resolve issues
Initiate non-conformance, deviation reports, engineering change orders (ECO) and follow up on necessary action items. Ensure that lab operations and workflow execution are compliant with ISO requirements. Drive completion of investigations and minimize disruptions to QC operations
Assist in root cause investigations for non-conforming lots and contribute to continual improvement efforts
Support process and product development activities, including process optimization, guard band and stability studies, and gauge R&R

What we offer

Equity grants
Comprehensive health and retirement benefit programs
Annual bonus program or sales incentive program
Health Package
Easy-to-use Benefits
Family oriented policies like parental leave
Generous Time Off

Fulltime

QC Associate Scientist I

The main function of a QC Associate Scientist is to perform microbiological qual...

Location

United Kingdom , Basingstoke

Salary:

12.00 - 13.00 GBP / Hour

Randstad

Expiration Date

April 27, 2026

Requirements

Qualified educationally to a Level 6 equivalent in a Microbiology or related subject (or QBE)
Has good numeracy skills, and the ability to read and follow methods / SOPs precisely
Has at experience of QC testing within a microbiology laboratory environment and ideally has experience in using SAP and MS Office software packages
Has experience in basic laboratory skills and techniques (pipetting, swabbing, streaking, pouring plates etc)
Consistently demonstrates our 4i Values of Integrity, Intensity, Innovation & Involvement
Puts the Customer First
Owns Their Results
Finds a Better Way Every Day

Job Responsibility

Carry out Quality Control Testing in accordance with Oxoid test specifications and methods
Plan, track and control the progress of products under test, and provide accurate availability dates to planning and customer services
Alerting the QC Team Leader of potential problems/failures and assist with further investigation
Ensure all test results are recorded within the SAP Quality Management module
Equipment checks and audits
Cleaning
Waste management
Consumable replenishing
Use of autoclaves
Ensure processes and procedures are carried out in accordance with the laboratory and company Quality Systems

Supervisor, Quality Assurance Internal Operations

Responsible for leading QA Associates, who provide QA support in the manufacturi...

Location

United States , Madison

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

BS degree in a scientific discipline
Minimum 5+ year’s relevant GMP experience
Knowledge of FDA/ISO regulatory requirements as well as industry trends
Computer knowledge, including Microsoft Office, Windows
Excellent interpersonal skills, must be able to lead and make decisions
College Level Mathematical Skills

Job Responsibility

Provide QA support for cGMP manufacturing operations
Coordinate with cross-functional teams to continually improve procedures with respect to area line clearances, labeling, packaging and material release
Support QA scheduling activities by monitoring the production, and visual inspection schedules and project management deliverables, and reviewing factors that may impact schedules
Oversee Quality System Events (QSEs) by verifying a Quality reviewer has been assigned to the QSE and monitor that the QSEs are being completed on time
Lead Associates in providing QA on the floor oversight of manufacturing
Oversee and assist employees with product / material labeling and disposition functions, routine manufacturing area line clearances, AQL Sampling and Inspection of Final Package Lots
Supervise the employees in the Quality Assurance Department
Ensure all training is performed by employees, including aseptic gowning, facility flow and visual inspection
Maintain Quality Metrics for the company
Review of master and executed raw material records. Release raw materials, as necessary

Fulltime

Associate Director, QC Manufacturing Support

We are seeking an Associate Director, QC Manufacturing Support to provide GMP ra...

Location

United States

Salary:

160000.00 - 180000.00 USD / Year

Apogee Therapeutics

Expiration Date

Until further notice

Requirements

BS or advanced degree in a relevant discipline (e.g., analytical chemistry, biochemistry, etc.)
10+ years of biotech industry experience in QC operations or analytical support roles
At least 6 years demonstrated experience supporting a GMP raw materials testing program
Understanding of analytical techniques relevant to monoclonal antibody testing
Experience in relationship management with external analytical test sites
Ability to effectively prioritize and manage multiple projects
Understanding of quality systems, cGMP regulations, and industry standards applicable to biopharmaceutical manufacturing and testing
Excellent communication skills
able to collaborate effectively across multidisciplinary teams
Successfully exhibit Apogee’s C.O.R.E. values: Caring, Original, Resilient and Egoless

Job Responsibility

Author internal raw materials testing specifications, specifically for non-compendial raw materials
Assess test methods being used by CDMOs for non-compendial raw materials to ensure they meet industry expectations for method verification and/or validation
Perform change control activities to ensure internal raw material specifications are updated and communicated to impacted test sites
Review and assess impact of vendor change notifications related to GMP raw materials
partner with internal and external stakeholders to development plans for material changes with major impact
Provide general analytical support to DS, DP, and MSAT teams in conjunction with QC Analytical Sciences on coordination and execution of in-process analytical testing
may include review of manufacturing-related sampling/testing plans, supporting materials and process-related risk assessments, (e.g., extractables/leachables, nitrosamines, etc.), sample shipment coordination, and analytical data review and management
Interface with internal and external stakeholders to support manufacturing campaigns at CDMOs, including supporting requests for information, document review, and audits/regulatory inspections as required
Support deviations, OOS/OOT/OOE investigations, and CAPAs related to GMP raw materials and in-process testing

What we offer

Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits
Three weeks PTO, two one-week company-wide shutdowns a year and dedicated paid sick leave
Commitment to growing you professionally and providing access to resources to further your development
Apogee offers regular all team, in-person meetings to build relationships and problem solve

Fulltime

QC Associate

Proclinical

Location:
Switzerland , Visp

Category:
Quality Control

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 19, 2026

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Job Posted:March 19, 2026

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