Operations Specialist supporting shop floor execution, batch closeout, and troubleshooting in a GMP manufacturing environment.
Compensation
The salary range for the primary location of this role is: $79,200.00 - $124,700.00. The successful candidate will be eligible for annual bonus and long‑term incentive, if applicable.
Responsibilities
Partnering with the Operations management team to create and execute strategies that support design, development, delivery and evaluation of projects related to steady‑state production and/or continual process improvement.
Authoring and reviewing documents and SOPs.
Batch Record Review.
eLog Review.
Lead safety investigations.
Requirements
High School Diploma
Bachelor’s degree in a technical field
Bachelor's degree in a direct GMP, biotechnology, manufacturing setting
Nice to have: Understanding of MPS methodologies
Nice to have: Experience with shop‑floor cGMP manufacturing and related systems (i.e. SAP)
An energetic individual responsible for supporting shop floor execution, batch closeout, and general troubleshooting.
Compensation
$79,200.00 - $124,700.00
Responsibilities
Partnering with the Operations management team to create and execute strategies that support design, development, delivery and evaluation of projects related to steady-state production and/or continual process improvement.
Authoring and reviewing documents and SOPs
Batch Record Review
eLog Review
Lead safety investigations
Requirements
High School Diploma
Bachelor’s degree in a technical field
Nice to have: Understanding of MPS methodologies
Nice to have: Experience with shop-floor cGMP manufacturing and related systems (i.e. SAP)
Nice to have: Familiarity with pharmaceutical regulatory requirements
The role supports the Durham manufacturing site by coordinating project activities, maintaining accurate project information, supporting change controls and incident writing, and helping teams complete actions to support PAI and filing.
Compensation
$79,200 - $124,700
Responsibilities
Support Pre-Approval Inspection (PAI) and filing-readiness plans by tracking deliverables, owners, due dates, dependencies, and open actions
Update readiness trackers and dashboards so milestones, risks, gaps, and recovery actions are visible and current
Coordinate meetings, prepare materials, document decisions, and follow up with owners on assigned actions
Help organize inspection evidence, procedures, training records, and filing-related documents for review by subject matter experts
Maintain project and portfolio records, including project status, priorities, milestones, risks, resource needs, and dependencies
Centrillion Technologies is seeking a highly motivated and skilled Research Associate - Synthetic Chemistry to join their chemistry team to design and synthesize complex organic molecules.
Compensation
The expected salary range for this position is between $50,000 to $75,000. Actual pay may be more or less than the posted range.
Responsibilities
Design of multi-step syntheses of intermediates, building blocks and final products.
The use of solid-phase and solution chemistry techniques
The thorough purification of the compounds and characterization of synthetic products.
Perform cGMP manufacturing operations in a biologics production facility, including setup, calibration, rework, quality testing, and process development.
Support GMP upstream or downstream manufacturing processes for bulk biologics from microbial and cell culture systems.
Compensation
The anticipated hourly rate for this position in MD is $33.65 – $38.46 Plus Bonus.
Responsibilities
Complete Batch Production Records under current Good Manufacturing Practices and document processes using Standard Operating Procedures and Batch Production Records
Generate operational protocols and internal or external documents including Standard Operating Procedures, Batch Production Records, deviations, and summary reports
Collaborate with Process Development and Manufacturing Sciences and Technology teams to transfer new projects into GMP
Generate and revise internal and external documents such as Standard Operating Procedures and Batch Records
Support initiation and closure of deviations; may lead departmental investigations and close deviations and Corrective and Preventive Actions
Requirements
High School diploma or General Education Diploma
Associate’s degree in a Scientific, Engineering, or Biotech field
Bachelor’s degree in a Scientific, Engineering, or Biotech field
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