Senior Specification Author and Data Systems Specialist Job at Nestlé Purina (Solon)

Senior Packaging Specification Specialist

This role exists to own, elevate and future proof packaging specification data, ...

Location

United Kingdom , Leeds

Salary:

Not provided

Unilever

Expiration Date

Until further notice

Requirements

Degree-level education in a scientific or engineering discipline
Strong R&D experience, with deep understanding of specifications and data quality
Proven experience managing specifications across their full lifecycle
Solid understanding of PLM / AWS and end-to-end data flows
Working knowledge of packaging legislation and regulatory frameworks
Experience leading complex workloads, priorities and continuous improvement initiatives
A data-driven mindset with relentless attention to detail
Strong understanding of packaging materials, test methods and quality evaluation
Ability to translate complex information into clear, actionable outputs
Confident problem-solver who thrives in cross-functional, global environments

Job Responsibility

End-to-end ownership of packaging specifications
Lead delivery of the global Packaging Specification programme, ensuring right-first-time execution across brands and business units
Create, amend, Approve and release fit-for-purpose packaging specifications using strong technical judgement and rigour
Ensure specifications enable safe manufacture, consistent quality and regulatory compliance throughout the product lifecycle
Set and drive best-in-class data quality standards for packaging specifications
Ensure full compliance with Unilever internal standards and global regulatory requirements
Identify data gaps, risks or inconsistencies and lead corrective actions
Protect brands and consumers by reducing the risk of non-compliance, penalties or reputational impact
Act as Packaging Specification SME and PLM / AWS Superuser
Partner with Digital R&D to improve system functionality, efficiency and data accuracy

What we offer

Competitive salary and pension scheme
Annual bonus
Subsidised gym membership
Discounted staff shop
Shares
Flexible and hybrid working environment
Wellbeing support including hubs, programmes and development opportunities
Family-friendly and inclusive workplace

Fulltime

Senior Specialist I/II, Analytical Instrument and Systems Qualification

The Quality Control (QC) Specialist I/II—Analytical Instrument Qualification is ...

Location

United States , Durham, NC

Salary:

140000.00 - 185000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Bachelor’s or Master’s degree required, preferably in a life science discipline with 10-12 years’ experience
Working understanding of various analytical techniques primarily flow cytometry, plate based assays, automated liquid handling, liquid chromatography, capillary electrophoresis, and next generation sequencing
Experience qualifying and sustaining a range of QC instruments (e.g., HPLC/UPLC, GC, CE, UV‑Vis, FTIR, TOC, qPCR/plate readers, balances, pH meters, osmometers, NGS, Flow Cytometers), including networked data systems and interfaces
Working knowledge of applicable regulatory expectations for e‑records/e‑signatures and computer systems (e.g., Part 11/Annex 11), with successful inspection support
Experience collaborating across multi‑site QC organizations and with equipment vendors to deliver validation to plan
Technical writing skills
Ability to work independently in a high-paced team environment, meet deadlines, and prioritize work from multiple projects
Advanced ability to communicate effectively with peers, department management and cross-functional peers
Documentation Excellence: Clear, complete, and audit‑ready authorship of URS, SIA, DIAS, CS, FDS, protocols, RTM, and QSR
Systems Thinking: Ability to define system boundaries, dependencies, and data flows

Job Responsibility

Lead or support onboarding of new analytical instruments, defining system boundaries, intended use, and qualification strategy in alignment with SIA and URS, including Draft, review, and secure approval of URS, SIA, DIAS, CS, and FDS deliverables
Author and execute IQ/OQ/IOQ/PQ protocols (as appropriate), ensuring test pre‑requisites, evidence, and deviations are documented and resolved prior to release for GMP use
Build and maintain the Requirements Traceability Matrix (RTM) to link requirements (URS/DIAS/CS/FDS) through protocol test cases and results
compile a Qualification Summary Report (QSR) to close projects
Define and verify data integrity and computerized system controls per DIAS (e.g., access management, audit trails, e‑records/e‑signatures, backup/recovery, calculations, data flows/interfaces) for instruments with embedded or attached control software
Initiate and/or execute change controls for instrument configuration changes, software upgrades, relocations, and method impacts
perform impact assessments and define re‑qualification needs
Perform/participate in periodic validation maintenance reviews to confirm lifecycle documents (SIA, URS, DIAS, CS, FDS, RTM, QSR) remain current and that assets stay in a validated state
Partner with QC SMEs, Digital Quality & Data Integrity, Validation, QA, IT, Facilities/Metrology, and vendors to plan and deliver qualification on schedule
coordinate service/vendor activities for installation, calibration, and PM in support of qualification and sustainment

Fulltime

New

Senior Privacy Impact Assessment PIA Specialist

We are seeking an expert Senior Privacy Impact Assessment (PIA) Specialist to le...

Location

Canada , Toronto

Salary:

Not provided

Randstad

Expiration Date

July 27, 2026

Requirements

Legislative Mastery: Comprehensive, professional-level knowledge of Canadian privacy frameworks, including FIPPA (and MFIPPA), PHIPA, and federal PIPEDA mandates, regulations, and associated jurisprudence
Digital Solution Assessment: Proven experience leading and conducting formal PIAs specifically tailored to online ecosystems, cloud configurations, and complex digital platforms
Health Information Expertise: Direct, hands-on experience managing assessments that involve Personal Health Information (PHI) crossing boundaries into third-party vendor applications or external systems
Modeling Capability: Demonstrated ability to read, interpret, and validate high-level data flow diagrams (DFDs) and business process models to identify privacy vulnerabilities
Interpersonal Skills: Elite consultation, negotiation, and report-writing capabilities, with a track record of driving cross-functional project teams toward a privacy consensus
Compliance Framework Knowledge: Strong familiarity with internationally accepted Fair Information Practices and the operational rulings of the Information and Privacy Commissioner of Ontario (IPC)

Job Responsibility

Privacy Impact Assessment Leadership: Lead the end-to-end development of PIAs to determine whether new technologies, cloud configurations, or business policies meet complex legal compliance requirements
Risk Mitigation Engineering: Evaluate information architectures and digital solutions to identify privacy threat vectors, design security countermeasures, and author formal privacy risk registries
Third-Party & Vendor Validation: Conduct rigorous privacy reviews on third-party application solutions, non-profit sector software providers, and external data service integration partners handling personal health information
Data Flow & Systems Auditing: Analyze complex systemic data flows, information architectures, and identity verification mechanisms to assess the current and future privacy implications of system designs
Policy Collaboration: Partner with policy development teams to review, compare, and draft privacy-enhancing guidelines, standard operating procedures, and governance baselines
Records Governance Oversight: Ensure compliance with information management directories, including strict data classification, secure retention schedules, and legal data disposition procedures
Cross-Functional Communication: Serve as a core advisor, translating dense legislative mandates and technical security patterns into plain language for executive sponsors, project managers, and business BAs

Fulltime

Senior Subsea Pipeline Marine Inspector

Airswift are a Global Manpower Provider specializing in the Energy, Infrastructu...

Location

Qatar , Doha

Salary:

Not provided

Airswift Sweden

Expiration Date

Until further notice

Requirements

Bachelor’s degree in engineering discipline (Mechanical) with demonstrated knowledge and experience
CSWIP 3.4UC Underwater Inspection Controller (Ref. CSWIP Document No.CSWIP-DIV-7-95 – Part 2)
Current / valid BOSIET, TBOSIET, FOET or TFOET certificate (Ref. OPITO requirements), as applicable, in conjunction with an offshore medical certificate
Experience in conducting QMS audits and QA verification programs for various project phases (i.e., Engineering, Procurement, Construction and Installation (specifically, the Repair / Installation of pipelines and their associated infrastructure) would be preferable
At least six (6) years of working experience in Quality Assurance and Control (QA/QC) within the Oil and Gas industry (i.e., onshore and offshore)
Should have a proven history as a lead 3.4UC underwater inspection controller within demanding subsea/offshore projects
Subsea pipeline project experience is highly desired, with emphasis on pipeline operations, integrity assurance/non-destructive testing (NDT) and inspection, maintenance and/or design and construction
Familiarity with marine vessel operations and the organisational responsibility of the (i) Offshore Construction/Installation Manger, (ii) Vessel Master, (iii) Diving and ROV Supervisors, (iv) Client Representative(s), (v) Certifying Authorities, etc.
Knowledge and working experience of underwater inspection (UWI) in the form of visual inspection and non-destructive testing (NDT) conducted by means of the intervention of diver(s) and/or remotely operated vehicle (ROV) or crewed submersible (i.e., either as a practitioner and/or as the result of training or certification conforming to the requirements of CSWIP Document No. CSWIP-DIV-7-95 – Part 1 and 2)
With respect to UWI and other related activities, shall be familiar with (i) relevant subsea applied inspection systems, (ii) recording and processing of data, (iii) quality assurance (QA), (iv) inspection planning and briefing, (v) the capabilities and limitations of divers/ROV’s and submersibles, and (vi) the care and deployment of equipment

Job Responsibility

Ensure compliance with QatarEnergy LNG systems and processes, including the Project Management System. Engage contractors and applicable third-party organisations with a professional approach and maintain a good working level relationship
Have a knowledge of the front end engineering design (FEED) deliverables and engineering study reports to support the implementation of the Project Quality Plan (PQP) and associated Procedures
Review the project Scope of work, to determine the nature, extent, and frequency of quality verification activities
Monitor, evaluate and report the inspection and testing status of the pipeline repair activities
Maintain interface relationships with Subsea Pipeline Repair Installation, and Inspection Contractors (including nominated specialist third-party Contractor organisation(s)), and the applicable regulatory focal points
especially, those functioning offshore
Review Contractor’s and Vendor’s quality reports / deliverables, in line with the project quality requirements
In conjunction with the QA/QC delegation operating offshore, verify that the repair activities are in accordance with approved documented information (i.e. procedures, specifications, detailed methodologies, etc)
Support the underwater inspection (UWI) activities during the offshore / subsea repairs, by means of the development of job records, preparation of daily reports, review of diver commentary and transfer into the written form, interpretate ROV camera footage and transfer into the written form and be able to produce an oral commentary of the daily activities, as and when required
Monitor the technical inspections, verification, certification and acceptance by Specialist Third Party Inspection (TPI) Contractor, as applicable, and develop the final documentation for each offshore campaign (i.e., PL-49, PL-75, PL-610 and PL-811)

Fulltime

Vice President - Client Tax Operations

Location

India , Chennai

Salary:

Not provided

Citi

Expiration Date

Until further notice

Requirements

Bachelor's degree in Accounting, Finance, Business, Information Systems, or a related field
7+ years of experience in tax operations, wealth management, financial services, or highly regulated environments
2–3+ years of people leadership experience, including managing senior specialists and/or managers
Deep subject‑matter expertise across IRS Chapters 3, 4, and 61
FATCA, CRS, CARF
W‑8 / W‑9 documentation
NRA and backup withholding
1099 and 1042‑S reporting
Demonstrated experience leading complex regulatory change, remediation, and transformation initiatives
Executive‑level communication skills with the ability to influence across Operations, Technology, Data, Risk, Compliance, Legal, and senior leadership

Job Responsibility

Serve as the primary tax SME for Citi Wealth, providing authoritative guidance across FATCA, CRS, CARF, IRS Chapters 3, 4, and 61, W‑8/W‑9 documentation, FATCA, NRA and backup withholding, and 1099/1042-S information reporting
Own Wealth‑specific tax interpretations and positions, ensuring consistency with enterprise standards while addressing Wealth client needs and risk tolerance
Act as a senior advisor to Wealth Client Services, Front Office partners, Legal, Risk and Compliance on client communications, disclosures, regulatory explanations, and sensitive tax‑related inquiries
Represent Citi Wealth in enterprise tax governance forums, regulatory discussions, and cross‑business working groups
Provide end-to-end strategic Wealth‑level oversight and governance across the full tax lifecycle for UHNW clients
Identify, analyze, and govern systemic tax exceptions and risk themes
Develop scalable business intelligence, analytics, and AI‑enabled strategies to proactively detect emerging issues
Ensure operational readiness and flawless delivery of cyclical tax events
Serve as a Wealth business escalation authority for complex client, operational, regulatory, and systemic tax issues
Design and oversee exception management and remediation strategies

Fulltime

Data Center Project Director

The Data Center Project Director leads the strategic management of complex data ...

Location

Luxembourg , Luxembourg

Salary:

Not provided

JLL

Expiration Date

Until further notice

Requirements

Bachelor's degree in Engineering, Architecture, Construction Management, or equivalent technical discipline
Master's degree preferred
Professional certifications such as PMP, P3O, or equivalent project management credentials
Data center-specific certifications (Uptime Institute, DCCA, or similar) highly valued
12+ years of progressive project management experience with minimum 8 years focused on data center or critical infrastructure projects
Proven track record managing data center projects from 10MW to 100MW+ capacity with project values exceeding €50M
Deep understanding of critical infrastructure systems including UPS, PDUs, CRAC/CRAH units, generators, fire suppression, and building management systems
Comprehensive knowledge of data center design standards, industry regulations, and commissioning processes
Experience with both new construction and live environment upgrades requiring zero-downtime execution
Understanding of hyperscale, colocation, and enterprise data center business models and operational requirements

Job Responsibility

Provide executive-level project leadership for data center developments valued from €50M to €500M+, including hyperscale, colocation, and enterprise facilities
Develop and execute comprehensive project strategies encompassing scope definition, timeline optimization, budget management, and resource allocation across multiple concurrent projects
Lead business development initiatives, including proposal development, client presentations, and strategic relationship management with key stakeholders
Drive continuous improvement initiatives to enhance project delivery methodologies and organizational capabilities
Serve as primary executive interface for C-level clients, investors, and key stakeholders throughout the project lifecycle
Facilitate strategic decision-making processes, manage expectations, and ensure alignment between project objectives and broader organizational goals
Coordinate with utility providers, regulatory authorities, and local governments to secure necessary approvals and infrastructure connections
Lead executive steering committee meetings and board-level project reviews
Oversee technical delivery of critical infrastructure systems including power distribution (up to 100MW+), advanced cooling systems, fire suppression, security systems, and backup power generation
Ensure compliance with industry standards including TIA-942, Uptime Institute Tier classifications, ASHRAE guidelines, and local regulatory requirements

What we offer

Entrepreneurial, inclusive culture
Total Rewards program reflecting commitment to helping you achieve your ambitions in career, recognition, wellbeing, benefits and pay

Fulltime

Senior Quality Specialist

Climeworks is a leading high-quality carbon removal provider, combining decades ...

Location

Switzerland , Opfikon

Salary:

Not provided

Climeworks

Expiration Date

Until further notice

Requirements

You hold a degree in Chemistry or Analytical Chemistry
an advanced degree is a plus and strong applied laboratory experience is essential
You bring at least five years of industrial experience in a relevant field such as specialty chemicals, polymers, resins, or advanced materials manufacturing, with a proven track record in quality control and quality assurance
You are confident with material characterization and release testing, for example GC, IC, HPLC, FTIR, TGA, BET surface area, moisture and elemental analysis, and particle size methods, and you choose fit for purpose methods for routine release and investigations
You have deep expertise in method validation and verification, including designing protocols, defining specifications and acceptance criteria, estimating measurement uncertainty and detection limits, and ensuring data integrity across the full data life cycle
You have proven expertise in building and maintaining inspection ready documentation, authoring SOPs, test methods and work instructions, and operating within ISO based quality frameworks in fast growing environments
You are experienced in planning and conducting supplier and manufacturer audits on QC topics, assessing quality systems and measurement capability, gathering evidence, and driving effective corrective and preventive actions through to closure
You work fluently with LIMS and SAP QM for sample management, specification control, results review and release workflows, and you collaborate confidently with suppliers, manufacturers, Procurement, Product Owners and Operations
You communicate clearly and pragmatically in English.

Job Responsibility

You ensure robust quality control and quality assurance for sorbent materials and related QC processes in a dynamic scale‑up environment
You plan and coordinate QC campaigns for sorbents and related materials
You oversee measurements to meet workload and timelines
You review and approve QC data within defined QC specifications and testing standards
You maintain inspection‑ready documentation and records in SAP QM and linked systems
You manage deviations and change controls arising from QC activities and QC‑owned processes
You are responsible for method validation activities
You identify bottlenecks across QC processes and documentation as well as data handling
You act as the QC technical interface to suppliers and manufacturers
You support Procurement with commercial and contractual topics

What we offer

25 paid vacation days every year
public holidays
Hybrid work setup
Up to 4 weeks of remote work annually within any EU country
Fair base pay paired with an equity package
Inclusive parental leave
Dedicated budget to invest in your professional growth
Referral rewards

Senior Physician, Patient Safety

Join our dynamic Patient Safety team as a Senior Physician where you'll leverage...

Location

United States; Canada , Remote; Alberta

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Experience in clinical medicine (general or specialist qualifications) which is expected to be kept up to date
Good knowledge of drug safety and the drug development process
Good knowledge/understanding of medical terminology
Relevant experience in pharmacovigilance/ Drug Safety/ Clinical Practice
3 - 5 years previous experience in pharmacovigilance and/or medical monitoring is required
US Board Certification/board eligibility or regional equivalent for Canada
Bachelor of Medicine, Bachelor of Surgery (MBBS) / Doctor of Medicine (MD)/ Medically qualified from an acknowledged Medical School
Completion of at least basic training in clinical medicine (residency, internship etc.)
Demonstrated success in technical proficiency and scientific creativity
Good presentation and verbal/written communication skills

Job Responsibility

Maintaining a good working knowledge of the Adverse event/Safety profile of assigned products, labeling documents, data handling conventions, client’s guidelines and procedures, and global drug safety regulations and guidelines
Maintaining an awareness of global regulatory requirements, reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting
Performing medical review of cases not limited to (including complex and challenging cases requiring expert judgement)), clinical trial, and literature cases including combination products {drug-device}) according to client/Parexel Standard Operating Procedures (SOPs
as applicable) and liaising with the client, as require
Writing Pharmacovigilance/Marketing Authorization Holder (MAH) comment and assessing company causality
Review appropriateness of medical content in narrative for medical coherence
Assessing seriousness, listedness / expectedness of reported events
Providing medical inputs to case processing team
Raising appropriate follow-up queries for relevant information from the reporter/HCP (Health Care Professional)
Review and verify appropriate selection of adverse events from source documents, assign appropriate Medical Dictionary for Regulatory Activities (MedDRA) code, review narrative

What we offer

Flexible approach to work that meets your personal needs
Work from home
Benefits vary by country
Investment in your professional and personal development

Select Country

Senior Specification Author and Data Systems Specialist

Job Description

Job Responsibility

Requirements

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