Lead sales efforts for Johnson Controls’ advanced building systems solutions, driving customer acquisition and revenue growth across multiple high‑impact industries.
Responsibilities
Offer technically complex and high‑end integrated solutions to customers
Provide consultative selling to director‑level and higher stakeholders
Collaborate with internal technical, business and functional teams during pre‑sales and tender phases
Identify and develop new opportunities and strategic sales with prestigious customers
Develop long‑term customer relationships
Requirements
Bachelor’s or master’s degree in Engineering (process, mechanical or electrical preferred)
Maintain cleanliness and hygiene standards within the pharmaceutical manufacturing environment, ensuring compliance with GMP guidelines and regulatory requirements.
Compensation
Pay: $21.00/hr
Responsibilities
Execute thorough cleaning and sanitization procedures for designated GMP areas
Adhere strictly to GMP guidelines and regulatory standards
Maintain accurate records of cleaning activities
Assist in maintenance of cleaning equipment
Follow safety protocols and use PPE
Requirements
Nice to have: previous GMP cleaning experience
Nice to have: pharmaceutical or healthcare industry experience
Help productieprocessen digitaliseren binnen een farmaceutische omgeving door elektronische batchrecords te maken, configureren in PAS-X en ondersteunen van MES-projecten.
Compensation
Je kan rekenen op een motiverend salaris, aangevuld met extralegale voordelen, inclusief bedrijfswagen (of alternatieve vergoeding).
Responsibilities
Aanmaken en onderhouden van elektronische batchrecords (EBR's).
Vertalen van productieprocessen naar Master Batch Records.
Configureren van productieprocessen in PAS-X.
Implementeren van CIP-, SIP-, leaktest-, media- en bufferprocessen.
Ondersteunen van verschillende MES-projecten binnen de productiesite.
Support the development of manufacturing processes by conducting experiments, analyzing data, and documenting results. Work closely with senior scientists and engineers to implement process improvements.
Compensation
74,503.35USD - 100,798.65 USD
Responsibilities
Developing and implementing pioneering and fit-for-purpose analytical methods for impurity release testing.
Performing analytical testing to evaluate residual process impurities in drug substance and drug substance intermediates
Preparing technical reports for investigations, product and impurity characterization, and regulatory submissions.
Documenting laboratory activities according to GMP guidelines
Generating, analyzing, and interpreting analytical data to support product development investigations, routine testing, and regulatory submissions
Requirements
Bachelor’s degree
Associate’s degree and 2 years of Scientific experience
High school diploma / GED and 4 years of Scientific experience
As an Associate Specialist Operations, you are involved in the production of chemical products, focusing on independent batch processes at pilot and laboratory scales as well as producing magnetic particles and chromatography materials under GMP guidelines.
Responsibilities
Perform chemical productions in batch processes independently at pilot and laboratory scale.
Produce magnetic particles and chromatography materials in compliance with applicable GMP guidelines.
Operate and monitor PLC-controlled systems during production processes.
Actively participate in transferring new processes into production and support the optimization of existing workflows.
Perform in-process controls, such as determining pH, conductivity, and residual moisture content.
Requirements
Chemikant
Chemisch-technischer Assistent (CTA)
Nice to have: Experience in chemical or pharmaceutical production
The Quality Analyst is responsible for product safety to deliver consumer requirements through adhering to safety and quality standards, maximising cost effectiveness, optimal running and equipment efficiency.
Compensation
Not only do we offer a competitive salary and pension scheme, we also offer an annual bonus, subsidised gym membership, a discounted staff shop and shares.
Responsibilities
Perform routine analysis of raw, intermediate, and finished products
Good working knowledge of QC procedures, Unilever GMP guidelines
Initiate OOS notifications and follow up investigations for RCA reasons
Perform routine equipment calibration and maintain control charts
Stock taking and submission of orders for laboratory consumables
Requirements
Bachelor's in a science related degree or equivalent
Nice to have: Experience in a manufacturing or technical environment (FMCG)
Nice to have: Manual Dexterity
Nice to have: Clear written and verbal communication skills
The role focuses on technology transfer for mucilage preparation within the gelatine department, involving equipment specification, installation, process validation, and training associates for new plant facilities.
Responsible for the after care of outbound and reverse logistics shipments, ensuring high-quality customer service and adherence to Health Canada and GxP requirements.
Responsibilities
Coordinate transportation shipments in accordance with client requirements, Health Canada regulations, GMP, GxP, and Kuehne+Nagel QSHE standards.
Manage shipment routing, carrier coordination, and transportation performance monitoring.
Ensure on-time delivery, shipment confirmation, and timely collection of Proofs of Delivery (PODs).
Investigate and resolve shipment discrepancies, including root cause analysis and corrective actions.
Act as the key liaison between warehouse operations, clients, carriers, end users, and internal management teams.
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