Quality Assurance Department – Quality Assurance Operations / P1–P3 / Seishin Plant (Kobe City)
Indexed description
Overall Job Purpose
- Responsible for product quality assurance of pharmaceutical and medical device manufacturing processes and product testing at the Seishin site
- GMP compliance for new product launches, establishment of quality assurance systems, and coordination with internal stakeholders; collaborate with domestic and global internal departments to build quality standards and assurance systems for the manufacturing site based on GQP and GMP
- Quality management as a manufacturing site for products marketed in Japan; review of manufacturing and testing records; management of deviations, change controls, and validation
- Investigation and reporting of quality information and product quality issues
- Regulatory inspection and audit support at the manufacturing site, as well as batch release activities
- Quality improvement activities in collaboration with internal overseas manufacturing sites
- At least 3 years of experience in manufacturing, quality testing, or quality assurance within the pharmaceutical, medical device, food, cosmetics, or chemical industries
- In consideration of employee well-being and productivity, the company sets a commuting limit of within 90 km from the nearest station to the employee’s residence and within 90 minutes travel time by public transportation using the most economical route. Applicants living beyond this range are generally expected to relocate within commuting distance (company-leased housing is available). This policy also applies in cases where commuting by car is permitted.
- Native-level proficiency in Japanese
- Basic English proficiency, with a willingness to further develop language skills
- Pharmacist license
Scope of Changes to Job Duties: May be assigned to all duties within the company.
Scope of Changes to Work Location: As part of future career development, there may be opportunities for assignments at the Kobe Head Office, Tokyo Branch, Seishin Plant, or overseas offices.
Compensation & Benefits
- Salary: Competitive and commensurate with experience in accordance with company policy.
- Allowances: Housing allowance, commuting/transportation allowance, and others.
- Salary Increase: Available.
- Bonus: Performance-based bonus paid once annually in March of the following year, based on individual and company performance.
- Working Hours: 8:45 AM – 5:30 PM
- Overtime Pay: Paid for non-exempt positions (“Staff” roles only).
- Flexible Working Hours (Flextime System): Available.Flexible hours between 5:00 AM – 10:00 PM (excluding the designated common break period). Minimum daily working hours: 4 hours (2 hours for half-day leave). Core/common break time: 12:00 PM – 1:00 PM
- Smoking Policy: No smoking permitted at the workplace (fully smoke-free environment).
- Two days off per week (Saturday and Sunday)
- National holidays
- Year-end/New Year holidays and summer holidays
- Annual paid leave and special leave (e.g., bereavement)
Retirement: Mandatory retirement at age 60.
Re-employment System: Available up to age 65.
Annual Paid Leave (Granted Upon Hire)
- January–June: 10 days
- July: 5 days
- August: 4 days
- September: 3 days
- October: 2 days
- November: 1 day
- December: 0 days
職務目的:
- 西神サイトにおける医薬品および医療機器の製造工程・製品試験に関する品質保証業務を担当する
- 新製品上市におけるGMP適合対応、品質保証体制の構築、および社内関係者との調整;GQP・GMPに基づく製造サイトの品質基準・保証体制の構築に向け、国内外の社内部門と連携する
- 日本国内で販売される製品の製造サイトとしての品質管理;製造・試験記録のレビュー;逸脱・変更管理・バリデーションの管理
- 品質情報および製品品質問題の調査・報告
- 製造サイトにおける規制当局査察・監査対応、ならびにバッチリリース業務
- 海外社内製造サイトと連携した品質改善活動
- 製薬・医療機器・食品・化粧品・化学品業界における製造、品質試験、または品質保証業務の経験3年以上
必須スキル・資格:(採用必須条件)
- 日本語ネイティブレベル
- 基本的な英語力、および語学力向上への意欲
- 薬剤師免許
従事すべき業務の変更の範囲 :当社業務全般
就業場所の変更の範囲 :将来のキャリアの一環として、神戸本社・東京支社・西神工場・ 海外オフィスでの勤務をする場合もありうる
<処遇>
【給与】 当社規定により優遇します。
【諸手当】住宅手当、通勤交通費など
【昇給】有り
【賞与】年一回 個人業績結果及び会社業績結果に基づく業績変動賞与を翌年3月に支給する。
【勤務時間】8:45~17:30
【時間外手当】”担当職”のみ支給
【清算制フレックス勤務】適応あり。フレキシブルタイム:5時~22時内で勤務。
(ただし、一斉休憩を除く)1日の必要最低労働時間:4時間(半日休暇時は2時間)
一斉休憩:12時~13時
【在宅勤務制度】有
【受動喫煙対策】あり 就業場所 全面禁煙
【休日休暇】完全週休2日制(土・日曜日)、祝日、クリスマス、年末年始・夏期
- 年間休日125日、年次有給休暇、慶弔等
【福利厚生】住宅援助制度、借上社宅制度、リリーグループ補償制度(医療費・歯科医療費補助
制度等)
【定年制】有(60歳)
【継続雇用制度】:有(65歳まで)
【有給休暇】
年途中で入社した社員に対する年次有給休暇は、次の入社月の区分に従い入社翌月1日に付与される。入社日にかかわらず、その年の12月31日をもって、勤続年数が1年経過したものとみなし、翌年1月1日に翌年度の年次有給休暇が付与される。
入社月 1-6月 7月 8月 9月 10月 11月 12月
付与日数 10 5 4 3 2 1 0
【試用期間】 6か月間 試用期間中での賃金の違いはありません。
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
#WeAreLilly
Create a free Caio profile to unlock more results and save your role and location preferences.
Unlock free search