PCI Pharma Services logo

Senior BAS Technician

PCI Pharma Services

Bedford, NHOnsitePosted 54 days ago
Full TimeSenior LevelOperations & Supply ChainCDMO
Original posting ↗

Summary

PCI Pharma Services is a global contract development and manufacturing organization (CDMO) that provides comprehensive pharmaceutical supply chain solutions to pharmaceutical and biopharmaceutical companies worldwide. Founded in 1991 and headquartered in Philadelphia, Pennsylvania, the company has established itself as a trusted partner in the healthcare industry, offering integrated services that span the entire drug development lifecycle. PCI specializes in drug development support, clinical trial supply management, contract drug manufacturing, sterile and non-sterile drug product packaging, and global pharmaceutical logistics. With a global footprint encompassing 30 GMP-compliant facilities across multiple continents, the company serves as a strategic partner that follows the molecule from early development through commercial launch. PCI's expertise enables clients to accelerate time-to-market while ensuring regulatory compliance and quality standards. The company's comprehensive service portfolio includes analytical services, formulation development, commercial manufacturing, packaging, supply chain management, and distribution, making it a one-stop solution for pharmaceutical companies seeking to outsource their development and manufacturing needs.

Job description

Essential Duties and Responsibilities

  • Maintain, Troubleshoot and diagnose automated control systems problems, working closely with Facilities Technicians, Maintenance Technicians and Engineering personnel.
  • Maintaining HEPA certifications and room balancing for Grade A – Grade D cleanroom spaces. This involves damper adjustments in the field or within the BMS software.
  • Use of multimeter and troubleshooting electrical circuits up to 120VAC.
  • Ability to read and interpret P&ID diagrams.
  • Maintain accurate service records, reports, and documentation
  • Order parts, manage tools, and ensure proper use and care of equipment.
  • Ensure well-documented on-time completion of CMMS documentation including logbook entries, Work Orders and Alarm audits.
  • Communicate with supply vendors to coordinate work while regularly updating leadership on project status.
  • Schedule preventative maintenance, respond to urgent repair calls, and work with Reliability Engineers in the creation of emergency preparedness plans.
  • Responsible for document changes to systems per change management procedures
  • Provide input and author SOPs and PM documents
  • Travel between all facilities to support all functional areas
  • Regular and reliable attendance on a full time basis [or in accordance with posted schedule].
  • Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
  • Embodies PCI Pharma Services cultural values and aligns daily actions with department goals and company culture.

Qualifications

  • High School Diploma required, Minimum of 5 to 8 years of relevant experience
  • Minimum of 4 years of BAS and/or Facilitates experience preferred.
  • Minimum of 4 years of HEPA certification/or testing experience preferred.
  • At least 3-5 years of cGMP experience strongly preferred.
  • Must be proficient in Microsoft Office applications with the ability to use multimedia, email, spreadsheets, database management software including internet software, presentation software, and spreadsheet software
  • Ability to enter and manage data, create reports, and effectively utilize Computerized Maintenance Management Software (CMMS).
  • Strong written and verbal communication skills.
  • Strong problem solving skills and ability to work independently and as a part of a team.
  • Ability to developed understanding of automation standards (including GAMP)
  • Ability to understand of pharmaceutical systems and processes

Requirements

  • High School Diploma required, Minimum of 5 to 8 years of relevant experience
  • Minimum of 4 years of BAS and/or Facilitates experience preferred.
  • Minimum of 4 years of HEPA certification/or testing experience preferred.
  • At least 3-5 years of cGMP experience strongly preferred.
  • Must be proficient in Microsoft Office applications with the ability to use multimedia, email, spreadsheets, database management software including internet software, presentation software, and spreadsheet software
  • Ability to enter and manage data, create reports, and effectively utilize Computerized Maintenance Management Software (CMMS).
  • Strong written and verbal communication skills.
  • Strong problem solving skills and ability to work independently and as a part of a team.
  • Ability to developed understanding of automation standards (including GAMP)
  • Ability to understand of pharmaceutical systems and processes

Company overview

PCI Pharma Services is a global contract development and manufacturing organization (CDMO) that provides comprehensive pharmaceutical supply chain solutions to pharmaceutical and biopharmaceutical companies worldwide. Founded in 1991 and headquartered in Philadelphia, Pennsylvania, the company has established itself as a trusted partner in the healthcare industry, offering integrated services that span the entire drug development lifecycle. PCI specializes in drug development support, clinical trial supply management, contract drug manufacturing, sterile and non-sterile drug product packaging, and global pharmaceutical logistics. With a global footprint encompassing 30 GMP-compliant facilities across multiple continents, the company serves as a strategic partner that follows the molecule from early development through commercial launch. PCI's expertise enables clients to accelerate time-to-market while ensuring regulatory compliance and quality standards. The company's comprehensive service portfolio includes analytical services, formulation development, commercial manufacturing, packaging, supply chain management, and distribution, making it a one-stop solution for pharmaceutical companies seeking to outsource their development and manufacturing needs.

Explore more jobs of your matchFind more biopharma roles with GetBioJob.