SHL Medical
SHL Medical is a world‑leading provider in the design, development, and manufacturing of advanced self‑injection devices. With a global team of 6,000 employees, we partner with leading pharmaceutical and biotech companies to deliver innovative autoinjectors, pen injectors, and other drug delivery systems that ensure effective treatment for patients. Headquartered in Switzerland since 2018, with key operations in Sweden, Taiwan, and the US, we are united by a commitment to innovation, impact, and growth. Together, we empower our people to develop solutions that make a meaningful difference in the lives of millions of patients while fostering a supportive, inclusive, and dynamic workplace for our colleagues.
Job Overview Supports Operations and Development by performing inspections or testing for materials or products, and maintains records documenting the activity.
Main Responsibilities
Perform quality control activities (Incoming Inspection, Line Clearance, Material Verification, In‑process Controls, CCIT, Additional Sampling, and Inspections or Testing) to support SHL Pharma’s manufacturing process, Stability, and ENPs.
Inspect in‑process materials and finished products per applicable procedures, protocols, and/or batch record requirements.
Perform product identification and traceability activities as required (e.g., Quarantine).
Perform device testing in support of product realization, stability studies, and validations.
Notify management of nonconforming material or test failures promptly.
Segregate nonconforming materials per applicable procedures.
Check that the assembly or production line adheres to standards and procedures.
Assist with the initiation of QMS documents such as Non‑conformance Investigations.
Comply with all quality, safety, and work rules and regulations.
Must be flexible to work a variety of schedules to meet business needs.
Perform other related duties as assigned.
Skills and Qualifications
Associate Degree in Science or related area (equivalent experience considered but preferred).
High School Diploma or GED required.
1–2 years in the pharmaceutical and/or medical device industry or equivalent.
Minimum 1 year of experience with inspection tools preferred.
Basic knowledge of ISO 13485, GMP, FDA Compliance, CAPA, and Risk Management.
Knowledge and experience conducting laboratory analyses supporting FDA‑regulated products (e.g., physical, functional, or chemical analyses).
Experience working with sampling plans.
Knowledge of Good Documentation Practices.
Knowledge of Good Manufacturing Practices.
Proficient in Microsoft products (Word, Teams, Excel).
Shift hours: 1:00 PM–9:30 PM, flexible to work overtime.
What We Offer
Competitive compensation package.
Modern working environment with state‑of‑the‑art facilities and technologies.
Challenging assignments in a fast‑growing and innovative industry.
Position in a dynamic, international team of highly skilled professionals.
Various opportunities for personal and professional development within a global organization.
Additional Details
Seniority level: Entry level
Employment type: Full‑time
Job function: Quality Assurance
Industry: Medical Device
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Job Overview Supports Operations and Development by performing inspections or testing for materials or products, and maintains records documenting the activity.
Main Responsibilities
Perform quality control activities (Incoming Inspection, Line Clearance, Material Verification, In‑process Controls, CCIT, Additional Sampling, and Inspections or Testing) to support SHL Pharma’s manufacturing process, Stability, and ENPs.
Inspect in‑process materials and finished products per applicable procedures, protocols, and/or batch record requirements.
Perform product identification and traceability activities as required (e.g., Quarantine).
Perform device testing in support of product realization, stability studies, and validations.
Notify management of nonconforming material or test failures promptly.
Segregate nonconforming materials per applicable procedures.
Check that the assembly or production line adheres to standards and procedures.
Assist with the initiation of QMS documents such as Non‑conformance Investigations.
Comply with all quality, safety, and work rules and regulations.
Must be flexible to work a variety of schedules to meet business needs.
Perform other related duties as assigned.
Skills and Qualifications
Associate Degree in Science or related area (equivalent experience considered but preferred).
High School Diploma or GED required.
1–2 years in the pharmaceutical and/or medical device industry or equivalent.
Minimum 1 year of experience with inspection tools preferred.
Basic knowledge of ISO 13485, GMP, FDA Compliance, CAPA, and Risk Management.
Knowledge and experience conducting laboratory analyses supporting FDA‑regulated products (e.g., physical, functional, or chemical analyses).
Experience working with sampling plans.
Knowledge of Good Documentation Practices.
Knowledge of Good Manufacturing Practices.
Proficient in Microsoft products (Word, Teams, Excel).
Shift hours: 1:00 PM–9:30 PM, flexible to work overtime.
What We Offer
Competitive compensation package.
Modern working environment with state‑of‑the‑art facilities and technologies.
Challenging assignments in a fast‑growing and innovative industry.
Position in a dynamic, international team of highly skilled professionals.
Various opportunities for personal and professional development within a global organization.
Additional Details
Seniority level: Entry level
Employment type: Full‑time
Job function: Quality Assurance
Industry: Medical Device
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