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Bms Pharmaceutical Jobs (NOW HIRING)

Strive Pharmacy

Automation Engineer (BMS/EMS)

Alachua, FL · On-site

$105K - $117K/yr

We started Strive because we believed the pharmaceutical industry was overdue for a more human ... Manage the BMS/EMS Architecture, ensuring robust communication between field devices (sensors ...

Strive Pharmacy

Automation Engineer (BMS/EMS)

Alachua, FL · On-site

$105K - $117K/yr

We started Strive because we believed the pharmaceutical industry was overdue for a more human ... Manage the BMS/EMS Architecture, ensuring robust communication between field devices (sensors ...

Strive Pharmacy

Automation Engineer (BMS/EMS)

Alachua, FL · On-site

$105K - $117K/yr

... pharmaceutical facility. This role ensures that critical HVAC systems, utility plants, and ... Manage the BMS/EMS Architecture, ensuring robust communication between field devices (sensors ...

247Hire

BMS Integration Engineer

Clayton, NC · On-site

$70 - $90/hr

BMS Integration Engineer Location: Clayton, NC Category ... Engineering & Technical Opportunity We're partnering with a rapidly expanding pharmaceutical ...

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How much do bms pharmaceutical jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for bms pharmaceutical in the United States is $19.78, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $21.88 per hour, depending on experience, location, and employer.

What is a BMS Pharmaceutical professional?

BMS Pharmaceutical jobs refer to positions within Bristol Myers Squibb (BMS), a global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines. These roles can range from research and development, clinical trials, regulatory affairs, manufacturing, to sales and marketing. Employees at BMS work on advancing treatments for serious diseases, including cancer, cardiovascular conditions, and immunologic disorders. The company offers opportunities for professionals with backgrounds in science, engineering, business, and healthcare to contribute to improving patient outcomes.

What are some typical cross-functional collaborations for a BMS Pharmaceutical professional, and how do they impact project success?

BMS Pharmaceutical professionals often work closely with teams such as clinical development, regulatory affairs, manufacturing, and quality assurance to bring new therapies to market. Effective collaboration ensures that research findings are translated smoothly into clinical trials, regulatory submissions are accurate, and products meet quality standards. Regular communication and joint problem-solving are key, as challenges often require input from multiple disciplines. These collaborations not only enhance project outcomes but also provide valuable learning and networking opportunities for career growth.

What are the key skills and qualifications needed to thrive as a pharmaceutical professional at BMS (Bristol Myers Squibb), and why are they important?

To thrive as a pharmaceutical professional at BMS, you generally need a relevant science degree (such as pharmacy, chemistry, or biology) and a strong understanding of drug development and regulatory standards. Familiarity with laboratory information management systems (LIMS), data analysis tools, and compliance certifications like Good Manufacturing Practice (GMP) are typically required. Excellent teamwork, attention to detail, and strong problem-solving skills help you excel in cross-functional, high-stakes environments. These competencies ensure the safe, effective, and compliant development of innovative medicines that improve patient outcomes.

What is the difference between Bms Pharmaceutical vs Pharmaceutical Sales Representative?

AspectBms PharmaceuticalPharmaceutical Sales Representative
Required CredentialsDegree in pharmacy, life sciences, or related field; licensing may be requiredBachelor's degree in life sciences, marketing, or related field; sales experience preferred
Work EnvironmentPharmaceutical manufacturing facilities, laboratories, quality controlCustomer-facing roles, hospitals, clinics, and healthcare settings
Employer & Industry UsagePharmaceutical companies, biotech firms, research organizationsPharmaceutical companies, medical device firms, healthcare providers

While Bms Pharmaceutical roles focus on drug manufacturing, quality assurance, and research within pharmaceutical companies, Pharmaceutical Sales Representatives primarily engage in promoting and selling pharmaceutical products to healthcare professionals. Both roles require knowledge of the industry but differ in daily tasks and work environments.

More about Bms Pharmaceutical jobs

What states have the most Bms Pharmaceutical jobs?

States with the most job openings for Bms Pharmaceutical jobs include:

What job categories do people searching Bms Pharmaceutical jobs look for?

The top searched job categories for Bms Pharmaceutical jobs are:

Bms Pharmaceutical jobs near you
Infographic showing various Bms Pharmaceutical job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $41,139 per year, or $19.8 per hour.

CSV / Validation Specialist - BMS

Spruce Infotech

Indianapolis, IN • On-site

Contractor

Re-posted 19 days ago

Job description

  • Lead the BMS validation lifecycle across all 8 LMF buildings, from URS authoring through Validation Summary Report and closeout.
  • Author and obtain approval for User Requirement Specifications (URS) for the Metasys BMS platform.
  • Engage JCI on Software Requirement Specifications (SRS) review and acceptance.
  • Develop and execute Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols.
  • Risk based approach adhering to Lilly Quality procedures.
  • Generate and maintain requirements traceability matrices (RTMs) linking requirements through design, testing, and acceptance.
  • Author Validation Summary Reports (VSR) documenting validation outcomes, deviations, and acceptance rationale.
  • Perform 21 CFR Part 11 gap assessments for electronic records, electronic signatures, and audit trail compliance across Metasys and AVEVA PI.
  • Coordinate with the Integration Engineer on alarm management validation (ISA 18.2) and OT cybersecurity validation (ISA/IEC 62443).
  • Validate OPC/UA integration between Metasys, AVEVA PI, and DeltaV QBMS.
  • Draft commissioning protocols and support system acceptance testing.
  • Draft and maintain SOPs related to BMS operations, operator training, and preventive maintenance.
  • Enroll systems into the periodic review program for ongoing validated-state maintenance.
  • Support audit readiness by ensuring validation documentation is inspection-ready and aligned with FDA, EMA, and Lilly corporate quality standards.
  • Provide support for data integrity assessments across BMS and historian systems.
  • Assist with commissioning and qualification (C&Q) activities for new BMS equipment.
  • Support remediation of validation findings from internal audits or regulatory inspections.
  • Advise on validation strategy for future BMS system upgrades and expansions.
  • Demonstrated experience in computer systems validation (CSV) for building management or automation and control systems in a pharmaceutical/GMP-regulated environment.
  • Strong knowledge of GAMP 5 methodology, V-model lifecycle, and risk-based validation approaches.
  • Experience with 21 CFR Part 11 compliance, including assessment of electronic records, electronic signatures, and audit trail requirements.
  • Proficiency in developing validation deliverables: VP, URS, FS, DS, IQ/OQ/PQ protocols, RTMs, and VSRs.
  • Experience with BMS, DCS, PLC/HMI, or historian systems in a manufacturing environment.
  • Strong understanding of FDA and EMA regulatory expectations for computerized system validation.
  • Direct experience validating JCI Metasys, Honeywell, Siemens, or similar BMS platforms.
  • Experience with AVEVA PI Historian, DeltaV, or OPC/UA integration validation.
  • Familiarity with ISA 18.2 alarm management and ISA/IEC 62443 cybersecurity standards.
  • Familiarity with data integrity principles (ALCOA+) and data governance frameworks.
  • Experience with Kneat, ValGenesis, or similar electronic validation management systems.

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