Full-Time

Maintenance Supervisor

Takeda

Takeda

10,001+ employees

Global biopharmaceutical firm; R&D-driven NMEs

Compensation Overview

$89.9k - $141.2k/yr

+ Incentives

Monroe, GA, USA

In Person

On-site in Social Circle, Georgia; 12-hour shifts; 2-2-3 schedule.

Bachelor's

Category
Building Systems & HVAC (1)
Required Skills
Data Analysis

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Requirements
  • Typically requires high school diploma or GED plus 6+ years of related experience or bachelors' degree in occupational health and safety, sciences, engineering or related field and 3+ years of related experience.
  • Some leadership experience preferred.
  • Knowledge of lab techniques, theory, and practical hands-on sampling and testing.
  • Knowledge of Microsoft Office Applications, SCADA, process control software and other computer base applications.
  • Must have demonstrated interpersonal and leadership skills with the ability to interface well with personnel of all levels.
  • Must be able to work and facilitate a team-oriented environment.
  • Must possess problem-solving skills.
  • Must have organizational and administrative skills.
  • Must have strong communication skills (both verbal and written).
  • Must have demonstrated ability to manage multiple priorities in a manufacturing setting and prioritize responsibilities of self and direct reports appropriately.
  • Must have the ability to analyze and interpret scientific and statistical data.
  • Must have ability to understand cGMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry.
  • Must have strong aptitude for operation and controls of utilities equipment and processes.
  • Proficient within CMMS, JDE and or Maximo
  • May be required to supervise multiple groups.
Responsibilities
  • Supervise, lead and coordinate utilities operation and maintenance shift crews.
  • Responsible for operation and maintenance of the utilities throughout facility on your shift.
  • Organize and review daily Work Orders (WO) and Preventative Maintenance (PM) work.
  • Maintain daily communications with planning, scheduling and manufacturing counterparts to ensure needs are met.
  • Facilitate and verify appropriate training for all employees on the shift (including but not limited to cGMPs, job skills, safety, etc.).
  • Efficiently coordinate the workflow and documentation of PMs and WOs.
  • Must be familiar with plant and divisional SOPs as related to positional and department responsibilities.
  • Review procedures and update them as necessary.
  • Ensure a safe work environment is maintained through adherence to safety guidelines and policies.
  • Must follow safety rules and ensure compliance with GA state and federal EPA regulation and laws. Specific responsible system repairs, upkeep, and maintenance managed within regulating agencies such as OSHA.
  • Continuously stay current with assigned SOPs and keep an up to date training file ensuring compliance with all applicable Standard Operating Procedures.
  • Ensure all mandatory training requirements are met, including annual EHS training, GMP refresher training and any applicable training requirements.
  • Maintain an on-going two-way performance dialogue with Manager and meet timelines for completing all mid and year-end reviews and development plans for self and direct reports.
  • Demonstrate continuous progress with respect to increasing job knowledge and proficiency in technical understanding/problem solving.
  • Maintain a positive, professional and customer-oriented attitude. Communicate any concerns related to safe work practices, hostile work environment, sexual harassment or any other type of employee misconduct directly to the supervisor, manager or human resources.
  • Analyze, propose and correct longer-term solutions to existing and repeating problems.
  • Inspect, monitor, assess and assure the facility and equipment remains cGMP compliant and in a constant state of audit readiness.
  • Order and Maintain chemical inventory
  • May perform other duties as assigned.
  • Work with manufacturing, quality, EHS, engineering, vendor/contractors, security and other department supervisors and management.
Desired Qualifications
  • Some leadership experience preferred.

Takeda is a global biopharmaceutical company focused on discovering and delivering medicines and vaccines to improve patient health. It relies on extensive research and development to create new molecular entities (NMEs) and bring them to market, aiming for up to 15 product launches through FY2024 from a pipeline of 11 NMEs. Revenue comes mainly from selling pharmaceutical products, supported by about 41,000 third-party suppliers worldwide. The company differentiates itself through a deep history (over 240 years), a broad portfolio of global brands, and a patient-centric approach that places patients’ needs at the center of its operations while pursuing environmental sustainability. Takeda’s goal is to advance health globally by turning scientific innovations into accessible therapies, maintaining long-term growth through steady product innovation and responsible operations.

Company Size

10,001+

Company Stage

IPO

Headquarters

Tokyo, Japan

Founded

1781

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Simplify Jobs

Simplify's Take

What believers are saying

  • Orzeyful launch opens a new neurology franchise with disease-modifying pricing power.
  • Takeda’s Q1 fiscal 2026 revenue rose 10.2% reported, driven by new launches.
  • Boltz partnership gives Takeda organization-wide AI access for structure prediction and generative design.

What critics are saying

  • Boston jurors found Takeda liable on May 18, 2026; appeal runs through 2026.
  • Takeda booked roughly 403.5 billion yen for Amitiza exposure, crushing fiscal 2025 profit.
  • Takeda will cut about 4,500 jobs in fiscal 2026, signaling integration strain after Shire.

What makes Takeda unique

  • Takeda’s Orzeyful became the first FDA-approved orexin therapy on August 5, 2026.
  • Takeda already won China approval for Orzeyful in July 2026, extending first-mover advantage.
  • Takeda’s dengue vaccine is India’s first approved Japanese dengue vaccine, strengthening emerging-market positioning.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

401(k) Retirement Plan

401(k) Company Match

Paid Vacation

Paid Sick Leave

Wellness Program

Tuition Reimbursement

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

0%

2 year growth

0%
Yahoo Finance
Aug 5th, 2026
FDA approves Takeda's Orzeyful, first medicine to treat underlying cause of narcolepsy type 1

The US Food and Drug Administration has approved Takeda's ORZEYFUL (oveporexton) for treating narcolepsy type 1 in adults. The oral medication is the first orexin receptor 2 agonist approved to address the underlying cause of the disease rather than individual symptoms. Narcolepsy type 1 is a chronic neurological disease affecting approximately 120,000 people in the US. It is driven by orexin deficiency and causes excessive daytime sleepiness, cataplexy, cognitive symptoms and disrupted sleep. Clinical trials showed adults taking ORZEYFUL experienced significant improvements across the full range of symptoms compared to placebo. Takeda is preparing for the US launch, which will proceed following completion of the Drug Enforcement Administration scheduling process. The company describes the approval as potentially redefining how narcolepsy type 1 is managed.

GeekWire
Jul 31st, 2026
AI drug developer Accipiter Bio quietly tops up seed round with $10.5M

Seattle-based biotech startup Accipiter Biosciences has raised an additional $10.5 million, less than a year after emerging from stealth with $12.7 million. The funding, from existing investors including Flying Fish Partners and Takeda, will accelerate the company's drug development programmes. The startup uses AI tools developed at the University of Washington's Institute for Protein Design to engineer proteins that can bind multiple cellular targets simultaneously. The company has expanded to 22 employees, including researchers who worked under Nobel laureate David Baker. Accipiter Bio has partnerships with Pfizer and Gilead Sciences-owned Kite Pharma, with potential milestone payments exceeding $330 million. The additional funding will enable the company to advance three or four drug candidates into clinical trials, focusing on immunology and oncology.

Yahoo Finance
Jul 30th, 2026
Takeda Pharmaceutical Q1 results on track as new launches offset mature product declines

Takeda Pharmaceutical reported first-quarter fiscal 2026 results aligned with its full-year outlook. Revenue totalled JPY 1.22 trillion, up 10.2% on an actual foreign-exchange basis but down 0.5% at constant exchange rates. Core operating profit reached JPY 358.9 billion, rising 11.5% on an actual FX basis. The company's core inline brands, representing 58% of total revenue, grew 2.3% at constant exchange rates. New launches accounted for 4% of revenue but grew 22.6%, supported by FRUZAQLA, LIVTENCITY, ADZYNMA and QDENGA. Takeda is preparing three product launches: ORZEYFUL for narcolepsy type 1, rusfertide for polycythemia vera, and zasocitinib for psoriasis. The company maintained its fiscal 2026 guidance and expects to generate JPY 650 billion to JPY 750 billion in free cash flow.

Nikkei Asia
Jul 21st, 2026
India approves first dengue vaccine from Japan's Takeda

India has approved Takeda Pharmaceutical's dengue vaccine, marking the country's first approved vaccine for the disease. The Japanese drugmaker received regulatory approval as authorities seek to combat dengue's accelerating transmission across India. Dengue, a mosquito-borne viral infection, poses a significant public health challenge in tropical regions. The approval represents a milestone in India's efforts to address the disease burden. The vaccine's introduction comes as dengue cases continue to rise in the country, making prevention efforts increasingly urgent for Indian health authorities.

Business Wire
Jun 24th, 2026
Julie Kim becomes Takeda's president and CEO as pharmaceutical giant prepares three major launches

Takeda has appointed Julie Kim as Representative Director, President and CEO, completing an 18-month transition. Shareholders elected Kim as an internal director during the company's 150th Annual General Meeting in Osaka, after which the Board appointed her to the top role. Former president and CEO Christophe Weber retired following the meeting. Kim joined Takeda in 2019 through the Shire acquisition and previously held roles including president of the Plasma-Derived Therapies Business Unit and president of the U.S. Business Unit. She brings over three decades of global healthcare experience. Shareholders also elected three new external directors: Bruce Broussard, Koichiro Kimura and Dr Paul Stoffels. Takeda's Board now comprises 11 members, with eight serving as external directors. The company plans three major launches over the next 12 months.