Raw Materials Controller Job at Bakkavor (Old Leake (near Boston))

Supervisor, QA Raw Materials

The Supervisor, QA Raw Materials is responsible for leading a team of QA Raw Mat...

Location

United States , Bedford

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in relevant scientific discipline with a minimum of 5+ years’ experience in related GMP industry working in Quality Assurance or Quality Control groups which support receipt, inspection, or release of materials
Equivalent combination of education and experience considered
Knowledge of USP and EP pharmacopoeias, and pharmaceutical raw material compendial testing
Knowledge of FDA regulations (i.e., 21CFR Part 210, 211 & 820) and some experience working with international regulations such as EU, ICH
Ability to apply basic scientific principles to solve operational and quality tasks
Experience with RCA, technical writing, and working with quality related investigations

Job Responsibility

Perform review of external documentation and internal GMP documentation associated with incoming raw materials, components, chemicals, excipients, and Active Pharmaceutical Ingredients (API)
Provide Quality Assurance oversight to Materials Management and Quality Control, ensuring that site SOP’s and raw material specifications are adhered to
Responsible for the review and analysis of test results
ability to interpret and comprehend scientific information and data related to QC Micro and QC Analytical testing
Initiation, review, and disposition or closure of raw material quality systems
Assist in the identification, isolation, and containment of potentially nonconforming materials
Assist in the identification and management of expired material
perform scrapping of materials with Materials Management
Assist Materials Management and Project Management with finished product shipments
Provide input, review, and approval of new and revised raw material specifications

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

Material Supply Chain Lead

The Material Supply Chain Lead is a newly created role responsible for coordinat...

Location

United Kingdom

Salary:

Not provided

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Experience logging and reporting safety incidents, hazard, and near misses
Experience working in warehouses or distribution centres, including loading and unloading goods following safe working practices
Experience operating forklift trucks (FLTs)
Must hold a Certificate of Competence to RTITB standards for an appropriate type of forklift truck (FLT)
Strong administrative skills, including data entry, tracking and record keeping
Strong knowledge of inventory control and Warehouse Management Systems (EFI Vision experience is preferred)
Experience conducting quality checks on goods received from suppliers
Good IT skills and confidence working with warehouse systems and Microsoft applications
Strong organisational and problem-solving skills, with the ability to manage multiple priorities
Good communication, teamwork and interpersonal skills and the ability to provide direction and instructions to others

Job Responsibility

Log and report safety incidents, hazards and near misses, while actively challenging unsafe behaviours
Participate in the root cause analysis of safety incidents and hazards, and support the development, implementation, and follow up of corrective and preventative actions
Manage the eƯicient unloading, storage and loading of raw material, ensuring product is stored and dispatched in full and in line with operational requirements
Manage a team to conduct quality checks on raw material deliveries received from Raw material Supplier, escalating any issues as required
Coordinate and oversee the booking of inbound and outbound raw material movements between the Raw material Supplier, Markham Vale North and Markham Vale Production
Work with the Supply Chain Manager to coordinate the flow of raw material to support production schedules, adjusting priorities as needed to meet operational demands
Use Warehouse Management Systems (EFI Vision) to manage inventory movements, data entry and tracking
Maintain inventory accuracy, including stock counts and reconciliation as required – in line with auditing regulations
Complete all required documentation accurately and on time, including delivery dockets, manifests and system entries
Communicate clearly with the Raw material Supplier and internal stakeholders, including Markham Vale North teams, Supply Chain, transport providers and Markham Vale Production

What we offer

Competitive salary & benefits, including annual leave, pension, and a Cycle to Work scheme
Ongoing training and development opportunities
24/7 confidential support for you and your family
Flexible working options and family-friendly policies
Guaranteed interview for candidates meeting essential criteria (Disability Confident Employer)

Material Planner

Location

China , Wuhan

Salary:

Not provided

Aptiv plc

Expiration Date

Until further notice

Requirements

High School or above
More than 5 years working experience
Preferred some experience & basic knowledge of material planning system, material planning, inventory control
Have the high sense of teamwork, good ability in communication

Job Responsibility

Manage long & short term rolling forecast for material
Regular supplier communication
Material shortage escalation
Control raw material inventory, ensure healthy inventory, no dead and slow moving stock
Coordinate to resolve material issue
Follow with suppliers and forwarders for order confirmation and exact pick-up and or shipping dates

Fulltime

Senior Associate Quality Assurance I

The new Amgen Advanced Assembly and Final Product Operation facility in Ohio is ...

Location

United States , New Albany

Salary:

86928.00 - 106536.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school/GED + 4 years of Quality and/or GMP Manufacturing experience
Associate’s + 2 years of Quality and/or GMP Manufacturing experience
Bachelor’s + 6 months years of Quality and/or GMP Manufacturing experience
Master's
Scientific degree in Life Sciences, Physical Sciences, Applied Engineering or Manufacturing Technologies
Experience in and knowledge of GMP/GCP operations or similarly regulated industry
Affinity with digital innovation, data sciences and Quality engineering
Experience with raw material receipt, inspection & sampling
Highly effective verbal and written communication skills, strong interpersonal skills
Great attention to detail and high degree of accuracy in GMP documentation

Job Responsibility

Implement raw material sampling and inspection activities, including completion of GMP documentation to support raw material disposition
Perform raw material disposition ensuring that all quality deliverables are met
Provide quality expertise & guidance and work with operations partners, supply chain and supplier quality management to resolve issues and ensure timely release of the raw materials
Own and review controlled documents, including Standard Operating Procedures (SOPs), Work Instructions and Forms
Own, investigate and approve quality records including deviations/CAPAs assuring adherence to procedural requirements and confirming assessments and evaluations of different collaborators are complete and accurate as needed
Find opportunities for continuous improvement and implement improvements in partnership with other operations teams
Provide support during GMP Quality audits & inspections
Support Lean Transformation and Operational Excellence initiatives

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models, including remote and hybrid work arrangements, where possible

Fulltime

QA/QC, IMS and Customer Interface Manager

Explore a world of opportunities with us. Look ahead with us and help shape inno...

Location

Thailand , Saraburi

Salary:

Not provided

Evonik Industries

Expiration Date

Until further notice

Requirements

Bachelor’s degree / Master’s degree in chemistry or chemical engineering
15-20 years working experience in chemical/pharma/FMCG industries as Quality Control Manager
Strong communication, collaboration, and networking abilities
Fluency in English, both written and spoken
Proficiency in Microsoft tools, Minitab, Six Sigma., etc.
Analytical and problem-solving skills
Ability to work effectively in a global, multicultural environment

Job Responsibility

Building safety awareness & observing safety adherence in all operations of QA/QC to ensure zero incidence by regular safety talks & safety rounds with team members
Reviewing and controlling raw materials’ quality compliance to ensure the right raw material input into the production process
Raw material new vendor development to reduce dependability on single supplier by assessing new vendor’s specification & process capabilities, sample analysis, trials at lab/plant
Reviewing and controlling FG quality in compliance to ensure the right product is produced as per customers’ requirements by evaluating FG quality, its consistency & process capabilities
Planning, executing all improvement activities for product development, quality improvement of all grades of H2O2 & PAA by conducting lab trials & coordinating with plant team for plant modifications, plan trials & ending with commercial production
Train & guide team for SPC analysis, identifying improvement opportunities & implementation
Identify areas for improvement and develop strategies to achieve quality KPIs
Collaborate with cross-functional teams, suppliers and internal & external stakeholders to address quality issues and drive continuous improvement initiatives
Product specific regulatory approvals as per customer need and application
Evaluate the annual performance of direct reports, identify gaps/OFIs for individuals help them overcome and develop people. Drive quality culture and develop people

What we offer

hybrid and flexible working environments with #SmartWork
performance-based remuneration
occupational health benefits
attractive career paths
high-quality development programs

Fulltime

Quality Control Technician

This position is for a QC Technician I, located in Surbourg (France), reporting ...

Location

France , Surbourg

Salary:

Not provided

H.B. Fuller

Expiration Date

Until further notice

Requirements

Knowledge of chemistry and quality control
Experience in the adhesives industry is an advantage
Good written and oral communication skills (French)
Good computer skills: Word, Excel, PowerPoint, Access, SAP
Rigorous, methodical, organized, and able to work under pressure
Excellent communication and persuasion skills
Ability to work independently
Knowledge of ISO 9001 would be an asset

Job Responsibility

Ensures that all safety protocols are followed and that proper maintenance is maintained
Handle all activities related to quality control of received raw materials, production products and finished products to meet customer requirements
Raw material inspection upon receipt: verify the presence of the certificate upon receipt or check the conformity of the materials
Authorize the use of the raw material or block its use if non-compliant, in consultation with the Quality Coordinator if necessary
Ensure that all equipment is calibrated as required
Work closely with production: review Process Orders and propose good manufacturing practices, perform analysis of production batch samples and, if necessary, provide adjustment instructions, perform analysis of finished products and authorize shipment to customers
Prepare the necessary documentation and create certificates of conformity, if required
After each instance of non-conformity, inform all relevant departments with the appropriate written documentation, in consultation with the Quality Coordinator if necessary
Organizes the handling of non-conforming products
Maintains an up-to-date inventory of analyzed samples of raw materials & finished products

Unloading operator

We are currently looking for a unloading operator to join our clients team locat...

Location

Canada , Huntingdon

Salary:

24.00 - 25.00 CAD / Hour

Randstad

Expiration Date

April 09, 2026

Requirements

Ability to lift, push & pull 30-50lbs
Ability to work in hot and cold environments
Must have good computer knowledge (Excel, SAP)
Must be ok working in confined spaces over a large amount of time
Ability to work daily in Huntingdon, Quebec
Ability to operate several different production machines
Ability to work both the day & night shift on 12h rotations

Job Responsibility

Operate diverse machines ...
Handling raw materials onto the production line
Quality control of raw material
Handling of raw agricultural products
Working in refrigerated and humid departments (hot in summer, cold in winter)

What we offer

Competitive salary starting at $24/hr-$25/hr based on experience
Potential for a lot of overtime
12h shifts
Start date: January 12th, 2026
Enjoy 3 day and 4 day weekends every week!
Located in Huntingdon, Quebec. Only 35-45 minutes from Vaudreuil-Dorion, Châteauguay et Beauharnois!
Weekly pay
Dental Insurance
Full insurance package
Paid Time Off

Fulltime

Raw Materials Controller

Bakkavor

Location:
United Kingdom , Old Leake (near Boston)

Category:
Logistics

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
February 16, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

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Raw Materials Controller

Bakkavor

Location:United Kingdom , Old Leake (near Boston)

Category:Logistics

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:February 16, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

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Job Posted:
February 16, 2026