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$93k–$124k/yr
Full-time
bachelor degree, professional certificate, postgraduate degree
13 Paid Holidays, Vacation Time, 401K Match, Medical Benefits, Dental Benefits, Vision Benefits
Posted 24d ago
~40 hrs/week
Responsibilities
Establish and manage the Industrial Hygiene programs at the Rockville Biopharma site to ensure compliance with safety regulations. This includes performing field measurements, conducting risk assessments, and driving continuous improvement in EHS performance.
Requirements
Requires a Bachelor's degree in Science, Engineering, or EHS with at least 4 years of experience in program development. Preferred qualifications include professional certifications such as CIH, CSP, or PE, and experience in the pharmaceutical or biotechnology industry.
Full job description
The Industrial Hygiene Manager is responsible for establishing, implementing, managing, and continuously improving the Rockville Biopharma site’s Industrial Hygiene programs. This role requires a broad knowledge of EHS compliance programs and specialty areas, including biological, chemical, and physical hazards.
The Industrial Hygiene Manager will provide guidance on budget management to support external services and operating expenses. The position includes both strategic EHS planning and a hands-on, tactical role in supporting site-wide EHS management systems, regulatory compliance, and adherence to industry best practices.
The role is responsible for driving the site’s industrial hygiene program and escalating risks to the site leadership team. The Industrial Hygiene Manager will ensure compliance with all applicable local, state, federal, and company safety regulations.
Additionally, the Industrial Hygiene Manager will drive continuous improvement in site EHS performance and serve as a key point of contact with regulatory agencies (e.g., OSHA, EPA, DOT) and internal EHS teams.
Key Responsibilities:
Perform industrial hygiene field measurements and safety evaluations.
Develop quantitative workplace assessment strategy in terms of frequency, duration, location and sampling technology to accurately evaluate worker exposure to gases, vapors, fumes, dusts/mists, noise, radiation, heat stress, and biological agents.
Develop ergonomic risk assessment strategies including task assessment prioritization, industrial and office ergonomic evaluations, and selection and prioritization of control measures.
Review and track investigations of injuries, illnesses, environmental releases, non-injury accidents and near-misses to ensure that they are effective, and that they identify and resolve root causes. Lead investigations into serious adverse events.
Provide timely, high quality EHS technical support
Design, conduct and oversee EHS training
Carry out regular workplace inspections to monitor compliance with site rules, procedures, etc.
Develop and manage an internal audit program to assess compliance with legal and company requirements and identify opportunities for improvement
Establish site EHS policies, objectives, key performance indicators and targets that reflect local needs and alignment with Samsung’s long term EHS strategy.
Monitor and analyze EHS performance and initiate action to support or correct trends
Establish programs to manage the site’s different EHS risks and impacts, coordinated within an overall EHS management system
Review change proposals (including capital projects and new product introductions) to identify potential EHS issues and participate in their resolution
Work collaboratively with colleagues at other Samsung Biologics sites in around the world to ensure that EHS best practices and lessons from adverse events are shared effectively.
Maintain local EHS policies and procedures that effectively describe the site’s EHS management system.
Ensure that necessary EHS information is reported to local regulators and to stakeholders within Samsung
Requirements:
Bachelor's Degree in a Science, Engineering, or EHS discipline
4 years of experience in EHS program development and implementation
Skills:
EHS management systems.
Thorough understanding of key regulatory requirements (eg OSHA, NIOSH, ANSI, NFPA, and EPA rules and regulations) and their application to a manufacturing and laboratory environment, particularly in the following key areas:
Excellent computer skills primarily with Microsoft Office Suite and Project
Highly effective written, oral and presentation skills
Ability to prioritize multiple demands, think strategically and successfully lead multiple simultaneous projects
Preferred Experience:
Pharmaceutical or biotechnology industry experience.
Professional certification of a Certified Industrial Hygienist (CIH)
Professional certification (e.g., PE, CHMM, CIH, CSP)
Advanced degree
The anticipated salary range for this position in Maryland is $93,000 to $124,000 plus annual bonus, when eligible. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Benefits:
·13 paid holidays
·Vacation time
·401K match
·Medical, dental and vision benefits effective day one of employment
Innovation, passion and an unwavering dedication to find breakthrough solutions in biomedicines.
Industry
Pharmaceutical Manufacturing
Company size
1,001-5,000 employees
Founded
2011
Headquarters
Songdo, Incheon
LinkedIn followers
75,049
Samsung Biologics is a fully integrated CDMO offering state-of-the-art contract development and manufacturing services. With proven regulatory approvals, the largest capacity, and the fastest throughput, Samsung Biologics is an award-winning partner of choice and is uniquely able to support the development and manufacturing of biologics products at every stage of the process while meeting the evolving needs of biopharmaceutical companies worldwide.
Offices: 300 Songdo Bio Way, Songdo, Incheon 21987, KR · 600 Gateway Blvd, San Francisco, California 94080, US · 100 Challenger Rd, New Jersey, New Jersey 07660, US · 260 Franklin St, Boston, Massachusetts 02110, US · Tokyo, Tokyo 102-0071, JP
Innovation, passion and an unwavering dedication to find breakthrough solutions in biomedicines.
Industry
Pharmaceutical Manufacturing
Company size
1,001-5,000 employees
Founded
2011
Headquarters
Songdo, Incheon
LinkedIn followers
75,049
Samsung Biologics is a fully integrated CDMO offering state-of-the-art contract development and manufacturing services. With proven regulatory approvals, the largest capacity, and the fastest throughput, Samsung Biologics is an award-winning partner of choice and is uniquely able to support the development and manufacturing of biologics products at every stage of the process while meeting the evolving needs of biopharmaceutical companies worldwide.
Offices: 300 Songdo Bio Way, Songdo, Incheon 21987, KR · 600 Gateway Blvd, San Francisco, California 94080, US · 100 Challenger Rd, New Jersey, New Jersey 07660, US · 260 Franklin St, Boston, Massachusetts 02110, US · Tokyo, Tokyo 102-0071, JP