Lims Project Manager Job at Magentus (London)

IT Project Manager - ELN Platforms (Electronic Lab Notebook) & Scientific Data Systems

The IT Project Manager – ELN, Scientific Data Platforms & Manufacturing Systems ...

Location

India , Hyderabad

Salary:

Not provided

NTT DATA

Expiration Date

Until further notice

Requirements

10-15+ years in IT delivery with program-level ownership
8+ years delivering ELN or scientific data platforms in regulated environments
5+ years of MES implementation or integration experience (e.g., batch execution, eBR)
5-8 years of GxP validation (CSV/CSA) ownership across lab and/or manufacturing systems
5+ years driving adoption across scientific and/or manufacturing organizations
5+ years integrating ELN with LIMS/CDS/SDMS AND/OR MES with lab systems
Proven decision-making authority (not support roles)
Notice Period: 30 Days

Job Responsibility

Lead full lifecycle: strategy → design → configuration → integration → validation → deployment → adoption → optimization
Own delivery across lab systems and manufacturing platforms (MES)
Align scientific data strategy with manufacturing execution and batch data flows
Deliver against measurable outcomes: Adoption, Data quality, Compliance, Cycle time
Translate experimental workflows (R&D, QC) and manufacturing processes into structured digital systems
Standardize experiment design (ELN) and batch records & execution workflows (MES)
Ensure traceability from development → production
Own CSV/CSA validation strategy across ELN, MES, integrated lab/manufacturing systems
Ensure compliance with GxP, 21 CFR Part 11, ALCOA+ principles
Accountable for audit readiness and validation documentation completeness

Fulltime

Project Manager

The Project Manager will play a key role in the Toronto Industrial Operations Pr...

Location

Canada , Toronto

Salary:

Not provided

Myticas Consulting

Expiration Date

Until further notice

Requirements

Strong project management experience, ideally within digital or systems implementation
Must have experience managing digital applications projects in a global manufacturing environment, preferred experience working in a pharmaceutical manufacturing environment
Experience with LIMS platforms (OneLIMS preferred) is a strong plus but not required
Ability to operate in a fast-paced, global environment
Excellent communication and stakeholder management skills
Another important factor is fluency in PowerPoint/visual aids.

Job Responsibility

Lead end-to-end project management for digital solution implementations
Drive timelines, stakeholder communication, and delivery milestones
Support the rollout and integration of OneLIMS across relevant functions
Collaborate with cross-functional teams within a global program structure
Prepare and provide presentations (a part of stakeholder management) as a part of hosting Steering Committees.

Parttime

IT Project Manager

Piper Companies is seeking an IT Project Manager to support technology initiativ...

Location

United States , Greensboro

Salary:

145000.00 - 156000.00 USD / Year

Piper Companies

Expiration Date

Until further notice

Requirements

7+ years of IT Project Management experience supporting complex enterprise technology initiatives
Strong hands‑on experience with MS Project and ideally Jira
Solid understanding of SDLC, Agile, project governance, and documentation best practices
Experience developing and executing project plans, schedules, scope statements, and resource plans
Preferred experience with MES, LIMS, QMS, engineering design platforms, or specification systems
Excellent communication and stakeholder‑management skills
Experience working in regulated or manufacturing environments is a plus

Job Responsibility

Develop and manage project plans, timelines, scope, and deliverables across multiple concurrent IT initiatives
Lead end‑to‑end project execution using hybrid SDLC and Agile methodologies while ensuring alignment with business and compliance requirements
Utilize MS Project and ideally Jira for scheduling, tracking, reporting, RAID management, and stakeholder communication
Collaborate with Engineering, Quality, Operations, IT Development, Cybersecurity, and PMO teams to maintain transparency and ensure project readiness
Identify project risks, issues, and dependencies
drive mitigation strategies and ensure timely resolution
Coordinate testing, deployment, cutovers, and stabilization activities in regulated manufacturing environments

What we offer

medical
vision
dental
PTO
paid holidays
sick leave (as required by law)

Fulltime

Project Manager

As the primary liaison between Magentus and our NHS client, the successful candi...

Location

United Kingdom , Manchester

Salary:

Not provided

Magentus

Expiration Date

Until further notice

Requirements

Extensive experience in project management experience of delivering software implementations into the NHS and other healthcare networks
Prince 2 or similar project management qualification
Extensive experience in Laboratory Information Systems (LIMS) implementation or management
Proficiency in project management methodologies and tools, with a keen attention to detail and a commitment to delivering high-quality results.

Job Responsibility

Develop and manage a comprehensive project plan in collaboration with the client, outlining key milestones, deliverables, and resource requirements
Deliver projects on time to the required customer specification and within agreed timelines and budgets
Liaise and manage relationships with all project stakeholders including Healthcare Organisations and other third-party suppliers where there is a Prime contractor involvement
Produce and maintain all project documentation in accordance with PRINCE2 methodology (e.g., Project Initiation Document, Highlight reports, Project Plans etc)
Provide weekly project updates for the Programme Manager (and Prime Contractor where required) highlighting any contentious issues / risks and project RAG status
Maintain the project risk logs, managing and mitigating our exposure to associated risks and escalate as appropriate
Ensure project documents and Customer sign offs on all phases of work are complete, current, and appropriately stored
Ensure all post project activities are completed and the project closure checklist is completed
Collaborate closely with all appropriate project stakeholders to ensure they have a clear understanding of the Project
objectives, timescales and that project team members fully understand their individual roles and responsibilities

What we offer

Hybrid working environment from Manchester (City Centre) – 3 days a week from the Office and 2 from home
25 days (increases with length of service up to 4 days) plus 8 bank holiday
Holiday purchase scheme via salary sacrifice
An extra day annual leave for your birthday
Enhanced Maternity Leave
Enhanced Paternity Leave
Religious holiday swap programme
Up to two days paid Volunteering days
Paid time off during the working day to donate blood
Pawrental Leave

Fulltime

Manufacturing Manager

The Amgen Thousand Oaks, Building 20 Drug Product Manufacturing facility directl...

Location

United States , Thousand Oaks

Salary:

106148.00 - 143612.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree OR Master’s degree and 3 years of drug product manufacturing or operations experience OR Bachelor’s degree and 5 years of drug product manufacturing or operations experience OR Associate’s degree and 10 years of drug product manufacturing or operations experience OR High school diploma / GED and 12 years of drug product manufacturing or operations experience
experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources

Job Responsibility

Staff selection, training, oversight, performance, and development
Schedule adherence for tasks including, but not limited to manufacturing, qualification, and maintenance activities
Participating as a role model in Lean culture and continuous improvement programs with responsibility to translate onto the manufacturing floor
Elevating critical and impactful events to senior management and make real time processing decisions
Ensuring standard operating procedures are accurate for performing unit operations, batch record review is completed accurately meeting disposition timelines, and non-conformances are initiated & closed with right the first time documentation
Using appropriate systems for job duties (SAP, QMTS, and LIMS etc.) and identifies and implements process and safety improvements
Communicate production floor and project work at different levels of management
Interacting with business partners and internal/external audit teams including regulatory agencies as required
Working with business partners to assist with scheduling of maintenance tasks, engineering evaluations, and quality investigations
Supporting the introduction of new products and technologies into the facility

What we offer

health and welfare plans for staff and eligible dependents
financial plans with opportunities to save towards retirement or other goals
work/life balance
career development opportunities
Retirement and Savings Plan with generous company contributions
group medical, dental and vision coverage
life and disability insurance
flexible spending accounts
discretionary annual bonus program
stock-based long-term incentives

Fulltime

Systems Administrator, Cell Manipulation Core Facility

The System Administrator III will work internal to the Cell Manipulation Core Fa...

Location

United States , Boston

Salary:

106000.00 - 123500.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Knowledge of lab safety and infection control
Knowledge of cell therapy processing, medical, hematologic, oncologic and scientific terminology
Knowledge of Web publishing, ODBC/JDBC interfaces and SQL
Knowledgeable of BOE template builder and ability to collaborate/train on the builder
Ability to assess workload and prioritize and delegate tasks
Ability to accommodate schedule adjustments, as well as off-shift and weekend assignments as workload dictates
Excellent customer service skills and demonstrated ability to develop effective internal working relationships with a diverse employee population
Strong project management skills
Demonstrated competence in managing system projects
Demonstrated competence in writing and executing validation plans

Job Responsibility

The System Administrator III will work internal to the Cell Manipulation Core Facility to manage systems across the Cell Therapy (CT) Networks by implementation and validation of computer systems impacting the department and CT program. The System Administrator III works in conjunction with the project teams from Partners Healthcare System and CMCF technical staff as well as working with DFCI and Partners IS on enterprise systems such as Epic and Sunquest. Systems will include, but are not limited to Partners Order Entry System for Biological Products (BOE/BPAA), Eceptionist, Sunquest, REES Environmental Monitoring systems, Internal Server systems, CMCF FileMaker Databases, FreezerWorks Bio-Repository system selected MES, and other internal systems such as Microsoft Access and Filemaker databases
Demonstrates knowledge of CMCF, clinical and laboratory workflow to incorporate and propose design consideration for CMCF applications
Examines existing business models and flows of data in CT and assists to implement and support the IT manufacturing solutions for the CMCF
Performs thorough data and system analyses and develops a risk-based analysis understanding
communicates the consequences that erroneous data could have on patient care
Creates and maintains the procedures for system use, maintenance, and validation documents for upgrades and continuity of care during down time
Identifies critical data and coordinating / consolidation of existing data systems into the appropriate secure database
Manages all internal computer systems used by the facility and assists in the compilation of relevant data as required for ongoing analysis and quality improvement
Manages the team that submits data to the CIBMTR either via OTTR registry agent or formsnet3
Assists in the implementation / management of software needs for various transfusion management activities for DF clinical lab and teams

Fulltime

Quality Lab Associate I - Environmental Monitoring

This is where your work makes a difference. At Baxter, we believe every person—r...

Location

United States , Marion

Salary:

68000.00 - 93500.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

B.S. degree in Microbiology, Biology, or related science
Minimum 1 year experience in Pharmaceutical/Medical Device industry preferred
Strong communication and project management skills
Possess knowledge of core manufacturing and support systems
Computer literate/knowledge of Microsoft office applications (Word, Excel)
Must have good interpersonal skills and able to work optimally and efficiently in a team-based environment
Proficient in the aseptic use and handling of media plates and swabs for EM sampling
Must be a dedicated individual who requires minimal direction
Attention to detail and strong organizational skills
Must have a basic understanding of laboratory instrumentation

Job Responsibility

Conduct microbiological analyses on raw materials, in-process and finished products
Use laboratory instrumentation and computer systems to collect and record data
Complete all testing, including special project / protocol testing in a timely following local procedures and cGMP regulations
Maintain data integrity and ensure compliance with regulatory agencies
Operate equipment such as SAS Air Sampler and Climet Particle Counter for the purpose of collecting air/particulate samples
Perform surface sample testing using plate and/or swab method
Collect water samples throughout the facility on a weekly/monthly basis
Perform weekly and monthly HEPA inspections to ensure integrity of HEPA filters in clean-rooms
Performs weekly Real Time Risk Assessments (RTRA) to identify potential contamination issues in clean-rooms
Perform IMD (Instantaneous Microbial Detection) Testing

What we offer

Medical, Dental and Vision coverage
160 hours of Paid Time Off and Paid Holidays
401K match
Employee Stock Purchase Program
Paid Parental Leave
Tuition Reimbursement
Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
2 Days a Year to Volunteer

Fulltime

Quality Lab Associate I - Environmental Monitoring (7pm-7am)

This is where you make a difference in our patients' safety. As a member of the ...

Location

United States , Marion

Salary:

68000.00 - 93500.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

B.S. degree in Microbiology, Biology, or related science
Minimum 1 year experience in Pharmaceutical/Medical Device industry preferred
Strong communication and project management skills
Possess knowledge of core manufacturing and support systems
Computer literate/knowledge of Microsoft office applications (Word, Excel)
Must have good interpersonal skills and able to work optimally and efficiently in a team-based environment
Proficient in the aseptic use and handling of media plates and swabs for EM sampling
Must be a dedicated individual who requires minimal direction
Attention to detail and strong organizational skills
Must have a basic understanding of laboratory instrumentation

Job Responsibility

Conduct microbiological analyses on raw materials, in-process and finished products
Use laboratory instrumentation and computer systems to collect and record data
Complete all testing, including special project / protocol testing in a timely following local procedures and cGMP regulations
Maintain data integrity and ensure compliance with regulatory agencies
Operate equipment such as SAS Air Sampler and Climet Particle Counter for the purpose of collecting air/particulate samples
Perform surface sample testing using plate and/or swab method
Collect water samples throughout the facility on a weekly/monthly basis
Perform weekly and monthly HEPA inspections to ensure integrity of HEPA filters in clean-rooms
Performs weekly Real Time Risk Assessments (RTRA) to identify potential contamination issues in clean-rooms
Perform IMD (Instantaneous Microbial Detection) Testing

What we offer

Medical, Dental and Vision coverage
160 hours of Paid Time Off and Paid Holidays
401K match
Employee Stock Purchase Program
Paid Parental Leave
Tuition Reimbursement
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Flexible Spending Accounts
educational assistance programs
commuting benefits

Fulltime

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Lims Project Manager

Job Description

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