Jobs in Middlesex Centre, ON and nearby (5,579 jobs)

Jobs within 25 km of Middlesex Centre, ON, Canada. Nearby towns and cities are included. Distances are straight-line, not driving distances.

5,579 listings · 1,144 employers Counted Nov 10, 2026. How we count

About these jobs

Employers hiring include Shoppers Drug Mart (208 listings), Loblaw Companies Limited (205 listings), The Canada Life Assurance Company (144 listings).

Common roles: Retail sales associate, Customer service representative, Cashier.

816 of these listings include employer-provided pay. Open a job to see its currency and pay period.

Advertised starting pay
Pay period	Median starting pay	Listings
CAD / hour	20.00	531
CAD / year	70,000.00	255

Employer-listed minimums from at least 10 listings per currency and pay period. These are advertised starting amounts, not employee salaries. Jobs without a minimum and unusual amounts are excluded.

Workplace classifications: 0% remote, 13% hybrid, 87% on-site, 0% not specified. Hybrid and on-site classifications may be inferred from descriptions. Check the original ad.

Based on the dated count above. Listings can change. How we count

Jobs in Middlesex Centre, ON and nearby

Within 25 km

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Added 2 months ago
DIETARY AIDE
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Catalent Pharma Solutions

Project Manager

Strathroy, ON, Canada
CAN-Strathroy ON Adair, Canada

The final salary offered to a successful candidate may vary within this range $85,000 – $115,000, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. · Full-time

Apply on catalent.wd1.myworkdayjobs.com About employer

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Job details

Pay: The final salary offered to a successful candidate may vary within this range $85,000 – $115,000, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc.
Job type: Full-time
Experience: 5+ years of experience in pharmaceutical manufacturing, biotech, or CDMO operations.
Posting language: English
Posted: Aug 31, 2026

Original job description

Project Manager

About Site

The newly launched manufacturing facility on Adair Blvd marks a pivotal expansion of Catalent’s Zydis® technology, a globally renowned, fast-dissolve oral dosage form that has transformed the lives of millions of patients worldwide. This is your opportunity to join a dedicated team at the forefront of pharmaceutical manufacturing. At Adair, you’ll play a vital role in the startup of a site built for innovation and excellence, from installation and qualification to regulatory approval and commercial manufacturing.

Position Summary

We have an opportunity for a Project Manager to join our team and lead a portfolio of complex, cross-functional business projects within Catalent Adair - Zydis®. You will ensure successful delivery of projects such as infrastructure upgrades, equipment acquisitions, technical transfer, process development, validation, and scale-up. This role involves managing timelines, resources, budgets, and stakeholder expectations while meeting quality, regulatory, and EH&S standards. You will play a key role in ensuring compliance with Catalent policies and driving project success in a cGMP-regulated CDMO environment.

Shift: Typical Working Hours will be Monday-Friday 8 AM - 4:30 PM Location: Adair, ON 100% Onsite

The Role

Lead end-to-end project planning, execution, and governance for multiple concurrent projects.
Develop integrated project plans covering technical, quality, regulatory, supply chain, and operational workstreams.
Drive project reviews, risk management, stage-gate decisions, and change control.
Ensure all activities comply with Good Manufacturing Practices, regulatory, and CDMO client expectations.
Manage expectations, provide regular status updates, and ensure transparency of risks and milestones.
Manage site capital expenditure budgets, forecasts, and cost tracking.
Support regulatory submissions, client audits, and authority inspections as required.
Identify risks, bottlenecks, and process inefficiencies within the project portfolio and drive mitigation plans.
Manage cross-functional teams and set expectations based on project timelines.
Lead internal and external project team meetings, facilitate decision-making, and drive execution to ensure key milestones and deliverables are achieved.
Foster accountability by monitoring progress, communicating expectations, and ensuring timely completion of assigned deliverables.
Other duties as assigned.

The Candidate

Minimum Requirements

Bachelor’s degree in Life Sciences, Engineering, Pharmacy, or a related field (advanced degree preferred).
5+ years of experience in pharmaceutical manufacturing, biotech, or CDMO operations.
Proven experience managing complex technical projects in a Good Manufacturing Practices environment.
Deep understanding of drug development, technology transfer, validation, and commercial manufacturing.
Strong financial acumen, including budget management and commercial awareness.
Excellent communication, stakeholder management, and negotiation skills.
Currently Catalent participates in the Ontario Immigrant Nominee Program (OINP) on a limited basis.
Candidates with non-Canadian credentials must provide an evaluation confirming Canadian equivalency as determined by the Alliance of Credential Evaluation Services of Canada such as WES.

Preferred Skills & Background

Formal project management training (Project Management Professional, PRINCE2, Agile) is an advantage.

Pay

Why You Should Join Catalent

Comprehensive Benefit Package (Health, Dental, Vision, & Life Insurance)
Group Retirement Savings – Registered Pension Plan (RPP) with employer contributions
Employee Reward & Recognition programs
Opportunities for professional and personal development & growth including tuition reimbursement

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Apply on catalent.wd1.myworkdayjobs.com About employer

More about this job

Responsibilities

Lead end-to-end project planning and execution for complex, cross-functional business projects within a cGMP-regulated environment. Manage site capital expenditure budgets, timelines, and stakeholder expectations while ensuring compliance with regulatory and quality standards.

Requirements

Requires a Bachelor's degree in Life Sciences, Engineering, or Pharmacy with at least 5 years of experience in pharmaceutical manufacturing or biotech. Candidates must possess strong financial acumen and proven expertise in managing technical projects within a regulated environment.

Skills

Project Management
Pharmaceutical Manufacturing
Biotech Operations
CDMO Operations
Good Manufacturing Practices
Budget Management
Stakeholder Management
Risk Management
Technical Transfer
Process Development
Validation
Regulatory Compliance
Capital Expenditure Management
Cross-functional Leadership
Negotiation
Strategic Planning

Benefits

Health Insurance
Dental Insurance
Vision Insurance
Life Insurance
Group Retirement Savings
Registered Pension Plan
Tuition Reimbursement
Employee Reward & Recognition Programs

Visa sponsorship

Not detected in the job text

Keywords

Project Manager
Zydis Technology
Pharmaceutical Manufacturing
Biotech
CDMO
cGMP
Infrastructure Upgrades
Equipment Acquisition
Technical Transfer
Process Development
Validation
Scale-up
Regulatory Approval
Capital Expenditure
Budgeting
Risk Management
Stage-gate
Change Control
Supply Chain
Compliance
Project Management Professional
PRINCE2
Agile
Life Sciences
Engineering
Pharmacy
Commercial Manufacturing
Stakeholder Management
Regulatory Submissions
Audit Support

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Work requirements

Jobs in Middlesex Centre, ON and nearby