Compliance Administrator (Fixed Term, Part-Time)

LGC Group · Quality Assurance and Regulatory Affairs

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Company Description

• ABOUT LGC STANDARDS:
• LGC Standards is a division of LGC Group, the UK’s designated National Measurement Institute for chemical and bioanalytical measurements. We are a leading global manufacturer and service provider of quality assurance and research tools, supporting analytical needs in more than 120 countries worldwide. We use our expertise to produce to the highest standards, including ranges produced under ISO/IEC 17025 and accredited to ISO 17034. Our wide range of reference materials and proficiency testing schemes is complemented by our experience in outsourcing and customs, enabling us to adapt quickly to provide tailored solutions that meet our customers’ analytical needs. We innovate and apply science in order to ensure the safety and integrity of products and services, in line with our vision of science for a safer world.

Job Description

Job Purpose 

The Compliance Administrator plays a key role in maintaining compliance with U.S. import, export, and controlled substance regulations. This position is responsible for the preparation and submission of regulatory filings, maintenance of compliance records, monitoring regulatory requirements, and ensuring product classification data is accurately managed across internal systems.

This is a 6 months fixed term, part-time position.

Key Responsibilities 

• Ensure compliance with all controlled substance regulations at the Manchester site.
• Maintain secure storage and handling procedures for controlled substances.
• Ensure controlled substances are clearly identified and segregated according to schedule classification and registration requirements.
• Maintain accurate controlled substance inventory records, including properly documented biennial inventories.
• Renew DEA registrations annually and manage updates to drug code registrations.
• Monitor DEA regulatory updates, including classification and procedural changes, and communicate relevant changes to the U.S. Compliance team.
• Manage import permit and declaration processes for the Manchester site, including application submissions and closures.
• Apply for DEA exemptions.
• Maintain and organize controlled substance documentation and records for both sites.
• Process DEA Form 222 requests for site purchases and customer transactions as required.
• Partner with Customer Support teams to ensure controlled substance orders are processed in accordance with regulatory requirements and that all necessary documentation (e.g., DEA Form 222, permits) is in place.
• Prepare and submit regulatory reports, including:
  • ARCOS monthly reporting
  • Quota applications, monitoring, and year-end reporting
  • DEA exemption reports (semi-annually)
  • Acetone, 2-butanone, and toluene reporting
• Monitor inbound shipments to the Manchester site to ensure timely customs clearance and assist with issue resolution when necessary.
• Cross-train with other Compliance Coordinators to provide coverage during absences and support team flexibility.
• Participate in additional compliance and operational activities as assigned.

Qualifications

Essential

• Basic experience in US compliance/Familiar with CBP, FDA, EPA, DEA and USDA regulations.
• Knowledge of import and export regulations.
• Understanding US controlled substance regulations and how to apply to facility and documentation at facility.

Preferred

• Associate’s degree in a relevant scientific field or equivalent applicable experience.
• Familiarity with organic chemistry a plus.

Competencies 

• Ability to interpret and apply policies and guidance documents.
• Demonstrated ability to work in a team atmosphere and to work independently.
• Good attention to detail, well organized, innovative.
• Highly self-motivated.
• Strong team player.
• Effective communicator.

Physical Requirements

• Occasionally lift and move materials weighing up to 30 pounds as part of regular job duties.
• Perform computer-based work that involves prolonged and repetitive use of a keyboard, mouse, and other office equipment.

Additional Information

ABOUT LGC:

LGC is a leading, global life science tools company, providing critical components and solutions into high-growth application areas across the human healthcare and applied market segments. Its high-quality product portfolio is comprised of critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers’ products and workflows and are valued for their performance, quality, and range.

Our values

• PASSION
• CURIOSITY
• INTEGRITY
• BRILLIANCE
• RESPECT

Equal opportunities

LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or parental status, religion, or belief. Short listing, interviewing and selection will always be carried out without regard these factors.

For more information about LGC, please visit our website www.lgcgroup.com

This position requires current U.S. work authorization. We are unable to sponsor or assume sponsorship for temporary visas (including H‑1B, H‑2B, OPT, O‑1, TN)

#scienceforasaferworld 

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