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Major Pharmaceuticals Jobs (NOW HIRING)

E*Pro, Inc.

Major Incident Management Lead

Burbank, CA · On-site

... Entertainment, Pharmaceutical, Health Care and service industries ensures our services are ... Permanent Full Time 8+ years of experience primarily in ITIL Incident and Major incident Management ...

Oso Home Care

Major Medical Collector HYBRID

Irvine, CA · On-site

$21 - $33.15/hr

The Major Medical Collector is responsible for managing complex insurance accounts receivable for ... Coordinate with physicians, pharmacists, nurses, authorization specialists, and intake staff to ...

Oso Home Care

Major Medical Collector HYBRID

Irvine, CA · On-site

$21 - $33.15/hr

The Major Medical Collector is responsible for managing complex insurance accounts receivable for ... Coordinate with physicians, pharmacists, nurses, authorization specialists, and intake staff to ...

US Government Jobs

Pharmacist

Bloomfield, NM · On-site

$50.75 - $61/hr

This position is considered as the major source of pharmaceutical clinical information and is expected to manage selected patients with chronic disease states, as well as providing pharmaceutical ...

US Government Jobs

Pharmacist

Supai, AZ · On-site

$55.75 - $67/hr

This position is considered as the major source of pharmaceutical clinical information and is expected to manage selected patients with chronic disease states, as well as providing pharmaceutical ...

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Major Pharmaceuticals information

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$200K

$237.5K

$271K

How much do major pharmaceuticals jobs pay per year?

As of Aug 20, 2026, the average yearly pay for major pharmaceuticals in the United States is $237,500.00, according to ZipRecruiter salary data. Most workers in this role earn between $218,500.00 and $256,500.00 per year, depending on experience, location, and employer.

What is a major pharmaceuticals job?

A Major Pharmaceuticals job typically refers to roles within large pharmaceutical companies that develop, manufacture, and distribute medications. These jobs can include positions in research and development, regulatory affairs, sales, marketing, and manufacturing. Employees in this field work to ensure drugs are safe, effective, and compliant with government regulations. Careers in Major Pharmaceuticals often require scientific knowledge, attention to detail, and collaboration across teams to bring treatments to market efficiently.

What are the key skills and qualifications needed to thrive in a major pharmaceuticals position?

To excel in a Major Pharmaceuticals position, candidates typically need a background in pharmaceutical sciences, regulatory compliance, and strong project management skills, often supported by a relevant degree or certification. Familiarity with industry-standard tools such as laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and FDA regulatory databases is common. Exceptional analytical thinking, teamwork, and effective communication set top performers apart in this field. These competencies ensure that pharmaceutical products are researched, developed, and delivered safely and efficiently within strict regulatory guidelines.

What are typical career advancement opportunities in major pharmaceuticals roles?

Professionals working in Major Pharmaceuticals often have access to well-defined career paths, starting from entry-level research or production roles and progressing to positions such as team lead, project manager, or regulatory affairs specialist. Advancement is commonly achieved through gaining experience, pursuing specialized training or certifications, and demonstrating leadership skills. Many pharmaceutical companies also offer cross-functional development, allowing employees to explore roles in areas like quality assurance, clinical trials, or marketing. This structure supports long-term career growth and the ability to diversify your expertise within the industry.

What cities are hiring for Major Pharmaceuticals jobs?

Cities with the most Major Pharmaceuticals job openings:

What are the most commonly searched types of Major Pharmaceuticals jobs?

The most popular types of Major Pharmaceuticals jobs are:

What states have the most Major Pharmaceuticals jobs?

States with the most job openings for Major Pharmaceuticals jobs include:

Major Pharmaceuticals jobs near you
Infographic showing various Major Pharmaceuticals job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $237,500 per year, or $114.2 per hour.

Lead Document Control Specialist

FST Technical Services

Lebanon, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 28 days ago

Job description


Lead Document Control Specialist (EIDA)
Major Pharmaceutical Construction Project | Lebanon, Indiana
 Join FST Technical ServicesFST Technical Services is seeking an experienced Lead Document Control Specialist to support a major pharmaceutical manufacturing construction project in Lebanon, Indiana. This is a high-profile, fast-paced assignment where document accuracy, quality, traceability, and compliance are essential to project success.
The ideal candidate will have hands-on experience using the EIDA software platform and the leadership ability to coordinate document control activities across owners, contractors, engineering teams, QA/QC, commissioning, and project stakeholders.
This position is open to qualified U.S. citizens/Permanent residents located anywhere in the country who are willing to travel and mobilize to the project site. Regular home trips are allowable based on project scope and timeline.What You'll DoAs the Lead Document Control Specialist, you will oversee project documentation throughout the construction lifecycle while ensuring compliance with client standards, quality requirements, and established document control procedures. Also support and help manage up to 3 offsite Doc Control Specialist working from our Durham, NC Life Science office.Primary Responsibilities
  • Lead onsite document control activities for a major pharmaceutical facility construction project.
  • Serve as the project subject matter expert for the EIDA document management software platform.
  • Manage engineering drawings, specifications, RFIs, submittals, change documentation, transmittals, turnover records, and other controlled project documents.
  • Maintain accurate document numbering, revision control, distribution, approval status, and complete traceability.
  • Coordinate document flow among the owner, EPC team, contractors, subcontractors, QA/QC, commissioning, qualification, and project management personnel.
  • Review incoming documentation for accuracy, completeness, formatting, naming conventions, and compliance before release or routing.
  • Develop and maintain document registers, status reports, overdue-item tracking, audit records, and turnover package logs.
  • Support construction completion, QA/QC inspections, commissioning, qualification, validation, and final project closeout activities.
  • Train, guide, and mentor additional document control personnel as project staffing needs expand.
  • Identify and implement process improvements that increase document quality, consistency, and efficiency.
Required Qualifications
  • 5+ years of document control experience supporting large industrial construction, engineering, or capital projects.
  • Direct, hands-on experience using EIDA document management software is required.
  • Experience supporting pharmaceutical, life sciences, biotechnology, semiconductor, or another highly regulated manufacturing environment.
  • Strong understanding of engineering documentation, construction workflows, document lifecycles, revision management, and project turnover requirements.
  • Experience managing large volumes of technical documentation across multiple contractors and project disciplines.
  • Strong organizational, communication, prioritization, and problem-solving skills.
  • Exceptional attention to detail and commitment to document quality and compliance.
  • Proficiency with Microsoft Office, including Excel, Word, Outlook, and Teams.
  • Ability to work effectively in a fast-paced, deadline-driven construction environment.
  • U.S. citizenship is required.
Preferred Qualifications
  • Previous experience supporting a pharmaceutical greenfield, brownfield, expansion, or campus construction project.
  • Experience supporting QA/QC, commissioning, qualification, validation, or project turnover teams.
  • Prior EPC, owner-side, construction management, or general contractor project experience.
  • Previous lead, supervisory, or team-coordination experience within a document control function.
  • Familiarity with FDA-regulated, GMP, or controlled-document environments.
Travel and Project Requirements
  • This is a travel-based position supporting the project in Lebanon, Indiana.
  • Candidates may live anywhere in the United States but must be willing to mobilize and remain near the project site for the assignment. Regular home trips are allowed based on project scope/timeline.
  • Ability to successfully complete client onboarding requirements, including background screening, drug testing, site orientation, and other project-specific requirements.
  • Flexibility to work the project schedule required to support construction and turnover milestones.
  • Completion of OSHA 10 is required prior to start of job.
Compensation and BenefitsFST offers a competitive compensation and benefits package designed to support experienced traveling professionals, including:
  • Competitive base salary based on experience.
  • Mobilization funds to support project relocation and startup expenses.
  • Monthly per diem for eligible traveling employees.
  • Comprehensive medical, dental, and vision insurance.
  • 401(k) retirement plan with company match.
  • Paid Time Off and company holidays.
  • Life and disability insurance.
Why FST?FST Technical Services supports the delivery of some of the world's most advanced pharmaceutical, life sciences, semiconductor, and mission-critical facilities. Our professionals work on complex projects where quality, technical excellence, collaboration, and accountability matter.
This opportunity is ideal for an experienced EIDA document control professional who wants to take a lead role on a landmark pharmaceutical construction project while receiving strong travel support and FST employee benefits.
Apply today to help deliver the next generation of pharmaceutical manufacturing facilities with FST Technical Services.
 

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