Validation & Engineering Group, Inc.

Integrated Pest Management (IPM) Specialist

Validation & Engineering Group, Inc.  •  Carolina, PR (Onsite)  •  16 days ago
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Job Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking an onsite IPM Specialist responsible for day-to-day pest prevention, monitoring, control, and compliance at a pharmaceutical manufacturing site, ensuring product protection and GMP/EHS compliance.:

  • Integrated Pest Management (IPM) Specialist

Description:

  • Strong knowledge of Integrated Pest Management (IPM) principles; such as prevention, monitoring, threshold-based interventions, least-toxic controls, and documentation.
  • GMP and cleanroom awareness; understands contamination risks, gowning/cleanroom behavior, segregation and controlled access. Specifically aware of protocols for materials movement and transport within the plant to prevent contamination of manufacturing areas (incoming materials, tote/box handling, and temporary staging).
  • Regulatory/compliance mindset. Familiarity with FDA, EU GMP, local health codes, and internal quality systems.
  • Technical problem solving; identifies root causes, implements corrective/preventive actions and engineering controls.
  • Attention to detail and documentation discipline: precise logs, trend analysis, and corrective action records consistent with GDP/data integrity.
  • Communication and teamwork: clear communicator in English and preferably Spanish; interacts effectively with QA, Facilities, Production and Contractors.
  • Safety and EH&S focus. Follows PPE, lockout/tagout, chemical handling and confined-space rules. Understands and enforces grounding/entry procedures (material grounding, static control, and controlled changeover) required to reduce contamination and pest ingress during material transfers.
  • Personnel contamination controls. Knowledgeable in measures to prevent carry-in of insects on personnel and clothing (gowning checks, footwear control, pre-entry inspections, and behavioral controls), and able to train staff on minimizing pest transfer risk during entry/egress and material handling.

Qualifications

  • Education: Associate degree in Entomology, Biology, Environmental Science, Pest Management or equivalent technical diploma. Bachelor's degree preferred.
  • Professional certification (preferable): Certified Pest Management Professional (CPM, BCE or equivalent) preferred; state/local pesticide applicator license where required.
  • Experience: Minimum 3–5 years of hands-on IPM experience in regulated manufacturing or food/pharma environments; at least 1 year of onsite, full-time IPM role preferred.
  • Technical skills: familiarity with rodent control, insect monitoring traps, fumigation basics, baiting strategies, sealing/exclusion methods, and safe use of approved pest control products.
  • Systems knowledge: experience with computerized maintenance/logging systems, basic Excel for trend analysis, and familiarity with CMMS or compliance systems is a plus.
  • Language: English required; bilingual (Spanish) strongly preferred.

Daily On-Site Activities and Responsibilities

  • Morning site inspection: perform perimeter and interior inspections (production areas, warehouses, waste areas, loading docks, HVAC intakes) and log findings.
  • Monitoring & trapping: check and service monitoring stations/traps, rodent bait stations, fly traps and glue boards; replace consumables and document counts/locations.
  • Trending & reporting: update daily logs and weekly trend charts; highlight threshold exceedances and submit immediate notifications to QA/Facilities.
  • Preventive actions: perform exclusion and housekeeping tasks (seal gaps, door sweeps, cleanup supervision), advise production/facilities on risk points.
  • Corrective interventions: execute approved treatments within GMP constraints (surface treatments, spot treatments, non-chemical options) under SOP and safety controls.
  • Contractor coordination: supervise/coordinate third-party pesticide applicators for scheduled treatments; ensure permits, certifications, and method statements are on file.
  • Documentation & compliance: maintain GMP-aligned records (daily logs, treatment records, material safety data sheets, certificates of analysis for pesticides if required), update IPM program files, and support audits.
  • Cross-functional engagement: attend daily/weekly production and facilities meetings; provide recommendations for engineering fixes and housekeeping improvements.
  • Training & awareness: deliver briefings to site staff on pest prevention (storage practices, waste handling, reporting suspected activity).
  • Emergency response: be available to respond to urgent pest incidents and execute rapid containment measures.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

Validation & Engineering Group, Inc.

About Validation & Engineering Group, Inc.

Validation & Engineering Group, Proudly serving our clients since 1997.

Our Mission states in part: "provide our clients with the best resources to meet their needs". In our search for the best talent, we are inclusive and do not discriminate. V&EG is proud to be an equal opportunity workplace and is an affirmative action employer.

Validation & Engineering Group provides world-class service and expertise to the pharmaceutical, medical device and biotechnology industries. We offer our clients: Validation, Control System Solutions, Instrumentation, Training, Equipment Rentals, and Regulatory Compliance Services to ensure adherence to Federal and European regulatory agencies. Our group had serve in solid dosages, liquids, creams, lyophilizers, and parenteral dosage.

Our agility in responding to our clients’ needs, access to the best pool of talent, and the combined experience and technical expertise of our resources make Validation & Engineering Group a leader in the pharmaceutical, medical devices, and biotechnology industries.

At Validation & Engineering Group we provide professional expertise in the areas of:

•Audit and Assessment

•Automated Process Control System Qualification

•Equipment and Facilities Qualification

•Facilities Start-Up and Commissioning

•GAP Analysis

•Information Systems Computer Validation

•Packaging and Process Analysis

•Process & Cleaning Validation

•Project Management

•Quality Systems

•Risk Based Approach

•Regulatory Compliance

•Standard Operating and Maintenance Procedures

•Training

•Utilities Support and Qualification

In addition we offer Equipment Rentals and training to your workforce such as: Temperature & Relative Humidity, Electrical, Process, Environmental, and. Analytical.

Our Offices:

Puerto Rico:

Centro Internacional de Mercadeo I 100 Carr. 165 Ste 703, Guaynabo, 00968 Puerto Rico

Phone: (787) 622-0996

United States:

2180 Satellite Blvd, Suite 400Duluth, Georgia 30097 United States

Phone: (770) 403-5802

Industry
Architecture & Engineering
Company Size
51-200 employees
Headquarters
Guaynabo, PR
Year Founded
1997
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